Canonical Allele Identifier: CA143799

Gene: DEPDC5

Linked Data

• ClinVar Variation Id: 50825
• ClinVar RCV Id: RCV000043585 ; RCV001387793 ; RCV003162360 ; RCV004545741
• dbSNP Id: rs587776977
• gnomAD v4: 22-31802739-C-T
• MyVariant Identifiers: chr22:g.32198725C>T (hg19) ; chr22:g.31802739C>T (hg38)
• PubMed: PMID:23542701 ; PMID:27683934

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.31802739C>T , CM000684.2:g.31802739C>T	GRCh38
NC_000022.10:g.32198725C>T , CM000684.1:g.32198725C>T	GRCh37
NC_000022.9:g.30528725C>T	NCBI36
NG_034067.1:g.53789C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382112.8:c.982C>T	ENSP00000371546.4:p.Arg328Ter
ENST00000400242.8:c.982C>T	ENSP00000383101.3:p.Arg328Ter
ENST00000400246.7:c.982C>T	ENSP00000383105.3:p.Arg328Ter
ENST00000400248.7:c.982C>T	ENSP00000383107.1:p.Arg328Ter
ENST00000400249.7:c.982C>T	ENSP00000383108.3:p.Arg328Ter
ENST00000433147.2:c.898C>T	ENSP00000410544.2:p.Arg300Ter
ENST00000535622.6:c.982C>T	ENSP00000440210.1:p.Arg328Ter
ENST00000642551.1:n.718C>T
ENST00000642684.1:c.*675C>T	ENSP00000494554.1:n.*675C>T
ENST00000642696.1:c.982C>T	ENSP00000495917.1:p.Arg328Ter
ENST00000642771.1:c.982C>T	ENSP00000496278.1:p.Arg328Ter
ENST00000642974.1:c.982C>T	ENSP00000496395.1:p.Arg328Ter
ENST00000643166.1:n.1069C>T
ENST00000643395.1:c.982C>T	ENSP00000496630.1:p.Arg328Ter
ENST00000643751.2:c.982C>T	ENSP00000495496.1:p.Arg328Ter
ENST00000644162.1:c.898C>T	ENSP00000495371.1:p.Arg300Ter
ENST00000644331.1:c.982C>T	ENSP00000494406.1:p.Arg328Ter
ENST00000645407.1:c.982C>T	ENSP00000496252.1:p.Arg328Ter
ENST00000645494.1:c.982C>T	ENSP00000495338.1:p.Arg328Ter
ENST00000645560.1:c.982C>T	ENSP00000495544.1:p.Arg328Ter
ENST00000645564.1:c.982C>T	ENSP00000494484.1:p.Arg328Ter
ENST00000645693.1:c.982C>T	ENSP00000496281.1:p.Arg328Ter
ENST00000645711.1:c.982C>T	ENSP00000493489.1:p.Arg328Ter
ENST00000645755.1:c.978C>T	ENSP00000495873.1:p.Thr326=
ENST00000645967.1:c.*450C>T	ENSP00000495187.1:n.*450C>T
ENST00000646465.1:c.982C>T	ENSP00000495655.1:p.Arg328Ter
ENST00000646515.1:c.982C>T	ENSP00000494700.1:p.Arg328Ter
ENST00000646701.1:c.898C>T	ENSP00000496158.1:p.Arg300Ter
ENST00000646755.1:c.982C>T	ENSP00000496532.1:p.Arg328Ter
ENST00000646969.1:c.982C>T	ENSP00000496724.1:p.Arg328Ter
ENST00000646998.1:c.982C>T	ENSP00000494662.1:p.Arg328Ter
ENST00000647343.1:c.898C>T	ENSP00000494879.1:p.Arg300Ter
ENST00000647438.1:c.898C>T	ENSP00000494714.1:p.Arg300Ter
ENST00000651528.2:c.982C>T MANE Select	ENSP00000498382.1:p.Arg328Ter
ENST00000382111.6:c.982C>T	ENSP00000371545.2:p.Arg328Ter
ENST00000382112.7:c.982C>T	ENSP00000371546.3:p.Arg328Ter
ENST00000400242.7:c.982C>T	ENSP00000383101.3:p.Arg328Ter
ENST00000400246.5:c.982C>T	ENSP00000383105.2:p.Arg328Ter
ENST00000400248.6:c.982C>T	ENSP00000383107.1:p.Arg328Ter
ENST00000400249.6:c.982C>T	ENSP00000383108.2:p.Arg328Ter
ENST00000473802.1:n.346C>T
ENST00000535622.5:c.982C>T	ENSP00000440210.1:p.Arg328Ter
NM_001007188.2:c.982C>T	NP_001007189.1:p.Arg328Ter
NM_001136029.2:c.982C>T	NP_001129501.1:p.Arg328Ter
NM_001242896.1:c.982C>T	NP_001229825.1:p.Arg328Ter
NM_001242897.1:c.982C>T	NP_001229826.1:p.Arg328Ter
NM_014662.4:c.982C>T	NP_055477.1:p.Arg328Ter
NR_110988.1:n.1184C>T
XM_005261862.1:c.982C>T	XP_005261919.1:p.Arg328Ter
XM_011530557.1:c.982C>T	XP_011528859.1:p.Arg328Ter
XM_011530558.1:c.982C>T	XP_011528860.1:p.Arg328Ter
XM_011530559.1:c.982C>T	XP_011528861.1:p.Arg328Ter
XM_011530560.1:c.982C>T	XP_011528862.1:p.Arg328Ter
XM_011530561.1:c.982C>T	XP_011528863.1:p.Arg328Ter
XM_011530562.1:c.982C>T	XP_011528864.1:p.Arg328Ter
XM_011530563.1:c.982C>T	XP_011528865.1:p.Arg328Ter
XM_011530564.1:c.982C>T	XP_011528866.1:p.Arg328Ter
XM_011530565.1:c.982C>T	XP_011528867.1:p.Arg328Ter
XM_011530566.1:c.982C>T	XP_011528868.1:p.Arg328Ter
XM_011530567.1:c.982C>T	XP_011528869.1:p.Arg328Ter
XM_011530568.1:c.982C>T	XP_011528870.1:p.Arg328Ter
XR_937972.1:n.1179C>T
XR_937973.1:n.1179C>T
NM_001007188.3:c.982C>T	NP_001007189.1:p.Arg328Ter
NM_001136029.3:c.982C>T	NP_001129501.1:p.Arg328Ter
NM_001242896.2:c.982C>T	NP_001229825.1:p.Arg328Ter
NM_001363852.1:c.982C>T	NP_001350781.1:p.Arg328Ter
NM_001363854.1:c.982C>T	NP_001350783.1:p.Arg328Ter
NM_001364318.1:c.982C>T	NP_001351247.1:p.Arg328Ter
NM_001364319.1:c.982C>T	NP_001351248.1:p.Arg328Ter
NM_001364320.1:c.982C>T	NP_001351249.1:p.Arg328Ter
NM_014662.5:c.982C>T	NP_055477.1:p.Arg328Ter
NR_110988.2:n.1188C>T
NR_146296.1:n.1088C>T
NR_157125.1:n.1067C>T
NR_157126.1:n.1071C>T
NR_157128.1:n.1188C>T
XM_011530557.2:c.982C>T	XP_011528859.1:p.Arg328Ter
XM_011530559.2:c.982C>T	XP_011528861.1:p.Arg328Ter
XM_011530561.2:c.982C>T	XP_011528863.1:p.Arg328Ter
XM_011530562.2:c.982C>T	XP_011528864.1:p.Arg328Ter
XM_011530563.2:c.982C>T	XP_011528865.1:p.Arg328Ter
XM_011530565.2:c.982C>T	XP_011528867.1:p.Arg328Ter
XM_011530568.2:c.982C>T	XP_011528870.1:p.Arg328Ter
XM_017029113.1:c.982C>T	XP_016884602.1:p.Arg328Ter
XM_017029114.1:c.982C>T	XP_016884603.1:p.Arg328Ter
XM_017029115.1:c.982C>T	XP_016884604.1:p.Arg328Ter
XR_001755389.1:n.1191C>T
XR_001755390.1:n.1191C>T
XR_937973.2:n.1191C>T
NM_001242896.3:c.982C>T MANE Select	NP_001229825.1:p.Arg328Ter
NM_001242897.2:c.982C>T	NP_001229826.1:p.Arg328Ter
NM_001363852.2:c.982C>T	NP_001350781.1:p.Arg328Ter
NM_001363854.2:c.982C>T	NP_001350783.1:p.Arg328Ter
NM_001369901.1:c.898C>T	NP_001356830.1:p.Arg300Ter
NM_001369902.1:c.898C>T	NP_001356831.1:p.Arg300Ter
NM_001369903.1:c.982C>T	NP_001356832.1:p.Arg328Ter
NR_146296.2:n.1071C>T
NM_001007188.4:c.982C>T	NP_001007189.1:p.Arg328Ter
NM_001136029.4:c.982C>T	NP_001129501.1:p.Arg328Ter
NM_001364318.2:c.982C>T	NP_001351247.1:p.Arg328Ter
NM_001364319.2:c.982C>T	NP_001351248.1:p.Arg328Ter
NM_001364320.2:c.982C>T	NP_001351249.1:p.Arg328Ter
NM_014662.6:c.982C>T	NP_055477.1:p.Arg328Ter
NR_157125.2:n.1067C>T
NR_157126.2:n.1071C>T