Canonical Allele Identifier: CA16608653
Gene: DEPDC5 HGNC NCBI

Linked Data

ClinVar Variation Id: 391802
ClinVar RCV Id: RCV000433181 RCV001038460
dbSNP Id: rs1057524233
MyVariant Identifiers: chr22:g.32179972G>A (hg19) chr22:g.31783986G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.31783986G>A , CM000684.2:g.31783986G>A GRCh38
NC_000022.10:g.32179972G>A , CM000684.1:g.32179972G>A GRCh37
NC_000022.9:g.30509972G>A NCBI36
NG_034067.1:g.35036G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000382112.8:c.562+1G>A ENSP00000371546.4:n.562+1G>A
ENST00000400242.8:c.562+1G>A ENSP00000383101.3:n.562+1G>A
ENST00000400246.7:c.562+1G>A ENSP00000383105.3:n.562+1G>A
ENST00000400248.7:c.562+1G>A ENSP00000383107.1:n.562+1G>A
ENST00000400249.7:c.562+1G>A ENSP00000383108.3:n.562+1G>A
ENST00000433147.2:c.478+1G>A ENSP00000410544.2:n.478+1G>A
ENST00000437411.6:c.563G>A ENSP00000416314.2:p.Gly188Asp
ENST00000458532.2:c.389G>A ENSP00000412057.2:p.Gly130Asp
ENST00000469974.6:c.229+1G>A ENSP00000494860.1:n.229+1G>A
ENST00000535622.6:c.562+1G>A ENSP00000440210.1:n.562+1G>A
ENST00000642551.1:n.298+1G>A
ENST00000642605.1:n.223G>A
ENST00000642684.1:c.*255+1G>A ENSP00000494554.1:n.*255+1G>A
ENST00000642696.1:c.562+1G>A ENSP00000495917.1:n.562+1G>A
ENST00000642771.1:c.562+1G>A ENSP00000496278.1:n.562+1G>A
ENST00000642974.1:c.562+1G>A ENSP00000496395.1:n.562+1G>A
ENST00000643166.1:n.649+1G>A
ENST00000643395.1:c.562+1G>A ENSP00000496630.1:n.562+1G>A
ENST00000643751.2:c.562+1G>A ENSP00000495496.1:n.562+1G>A
ENST00000644162.1:c.478+1G>A ENSP00000495371.1:n.478+1G>A
ENST00000644331.1:c.562+1G>A ENSP00000494406.1:n.562+1G>A
ENST00000645015.1:c.563G>A ENSP00000494299.1:p.Gly188Asp
ENST00000645407.1:c.562+1G>A ENSP00000496252.1:n.562+1G>A
ENST00000645494.1:c.562+1G>A ENSP00000495338.1:n.562+1G>A
ENST00000645560.1:c.562+1G>A ENSP00000495544.1:n.562+1G>A
ENST00000645564.1:c.562+1G>A ENSP00000494484.1:n.562+1G>A
ENST00000645693.1:c.562+1G>A ENSP00000496281.1:n.562+1G>A
ENST00000645711.1:c.562+1G>A ENSP00000493489.1:n.562+1G>A
ENST00000645755.1:c.562+1G>A ENSP00000495873.1:n.562+1G>A
ENST00000645785.1:n.428+1G>A
ENST00000645967.1:c.*30+1G>A ENSP00000495187.1:n.*30+1G>A
ENST00000646465.1:c.562+1G>A ENSP00000495655.1:n.562+1G>A
ENST00000646515.1:c.562+1G>A ENSP00000494700.1:n.562+1G>A
ENST00000646701.1:c.478+1G>A ENSP00000496158.1:n.478+1G>A
ENST00000646755.1:c.562+1G>A ENSP00000496532.1:n.562+1G>A
ENST00000646969.1:c.562+1G>A ENSP00000496724.1:n.562+1G>A
ENST00000646998.1:c.562+1G>A ENSP00000494662.1:n.562+1G>A
ENST00000647343.1:c.478+1G>A ENSP00000494879.1:n.478+1G>A
ENST00000647438.1:c.478+1G>A ENSP00000494714.1:n.478+1G>A
ENST00000651528.2:c.562+1G>A MANE Select ENSP00000498382.1:n.562+1G>A
ENST00000382111.6:c.562+1G>A ENSP00000371545.2:n.562+1G>A
ENST00000382112.7:c.562+1G>A ENSP00000371546.3:n.562+1G>A
ENST00000400242.7:c.562+1G>A ENSP00000383101.3:n.562+1G>A
ENST00000400246.5:c.562+1G>A ENSP00000383105.2:n.562+1G>A
ENST00000400248.6:c.562+1G>A ENSP00000383107.1:n.562+1G>A
ENST00000400249.6:c.562+1G>A ENSP00000383108.2:n.562+1G>A
ENST00000458532.1:c.162G>A
ENST00000535622.5:c.562+1G>A ENSP00000440210.1:n.562+1G>A
NM_001007188.2:c.562+1G>A NP_001007189.1:n.562+1G>A
NM_001136029.2:c.562+1G>A NP_001129501.1:n.562+1G>A
NM_001242896.1:c.562+1G>A NP_001229825.1:n.562+1G>A
NM_001242897.1:c.562+1G>A NP_001229826.1:n.562+1G>A
NM_014662.4:c.562+1G>A NP_055477.1:n.562+1G>A
NR_110988.1:n.764+1G>A
XM_005261862.1:c.562+1G>A XP_005261919.1:n.562+1G>A
XM_011530557.1:c.562+1G>A XP_011528859.1:n.562+1G>A
XM_011530558.1:c.562+1G>A XP_011528860.1:n.562+1G>A
XM_011530559.1:c.562+1G>A XP_011528861.1:n.562+1G>A
XM_011530560.1:c.562+1G>A XP_011528862.1:n.562+1G>A
XM_011530561.1:c.562+1G>A XP_011528863.1:n.562+1G>A
XM_011530562.1:c.562+1G>A XP_011528864.1:n.562+1G>A
XM_011530563.1:c.562+1G>A XP_011528865.1:n.562+1G>A
XM_011530564.1:c.562+1G>A XP_011528866.1:n.562+1G>A
XM_011530565.1:c.562+1G>A XP_011528867.1:n.562+1G>A
XM_011530566.1:c.562+1G>A XP_011528868.1:n.562+1G>A
XM_011530567.1:c.562+1G>A XP_011528869.1:n.562+1G>A
XM_011530568.1:c.562+1G>A XP_011528870.1:n.562+1G>A
XR_937972.1:n.759+1G>A
XR_937973.1:n.759+1G>A
NM_001007188.3:c.562+1G>A NP_001007189.1:n.562+1G>A
NM_001136029.3:c.562+1G>A NP_001129501.1:n.562+1G>A
NM_001242896.2:c.562+1G>A NP_001229825.1:n.562+1G>A
NM_001363852.1:c.562+1G>A NP_001350781.1:n.562+1G>A
NM_001363854.1:c.562+1G>A NP_001350783.1:n.562+1G>A
NM_001364318.1:c.562+1G>A NP_001351247.1:n.562+1G>A
NM_001364319.1:c.562+1G>A NP_001351248.1:n.562+1G>A
NM_001364320.1:c.562+1G>A NP_001351249.1:n.562+1G>A
NM_014662.5:c.562+1G>A NP_055477.1:n.562+1G>A
NR_110988.2:n.768+1G>A
NR_146296.1:n.668+1G>A
NR_157125.1:n.651+1G>A
NR_157126.1:n.651+1G>A
NR_157128.1:n.768+1G>A
XM_011530557.2:c.562+1G>A XP_011528859.1:n.562+1G>A
XM_011530559.2:c.562+1G>A XP_011528861.1:n.562+1G>A
XM_011530561.2:c.562+1G>A XP_011528863.1:n.562+1G>A
XM_011530562.2:c.562+1G>A XP_011528864.1:n.562+1G>A
XM_011530563.2:c.562+1G>A XP_011528865.1:n.562+1G>A
XM_011530565.2:c.562+1G>A XP_011528867.1:n.562+1G>A
XM_011530568.2:c.562+1G>A XP_011528870.1:n.562+1G>A
XM_017029113.1:c.562+1G>A XP_016884602.1:n.562+1G>A
XM_017029114.1:c.562+1G>A XP_016884603.1:n.562+1G>A
XM_017029115.1:c.562+1G>A XP_016884604.1:n.562+1G>A
XR_001755389.1:n.771+1G>A
XR_001755390.1:n.771+1G>A
XR_937973.2:n.771+1G>A
NM_001242896.3:c.562+1G>A MANE Select NP_001229825.1:n.562+1G>A
NM_001242897.2:c.562+1G>A NP_001229826.1:n.562+1G>A
NM_001363852.2:c.562+1G>A NP_001350781.1:n.562+1G>A
NM_001363854.2:c.562+1G>A NP_001350783.1:n.562+1G>A
NM_001369901.1:c.478+1G>A NP_001356830.1:n.478+1G>A
NM_001369902.1:c.478+1G>A NP_001356831.1:n.478+1G>A
NM_001369903.1:c.562+1G>A NP_001356832.1:n.562+1G>A
NR_146296.2:n.651+1G>A
NM_001007188.4:c.562+1G>A NP_001007189.1:n.562+1G>A
NM_001136029.4:c.562+1G>A NP_001129501.1:n.562+1G>A
NM_001364318.2:c.562+1G>A NP_001351247.1:n.562+1G>A
NM_001364319.2:c.562+1G>A NP_001351248.1:n.562+1G>A
NM_001364320.2:c.562+1G>A NP_001351249.1:n.562+1G>A
NM_014662.6:c.562+1G>A NP_055477.1:n.562+1G>A
NR_157125.2:n.651+1G>A
NR_157126.2:n.651+1G>A
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