Canonical Allele Identifier: CA2401709323

Gene: DEPDC5

Linked Data

• dbSNP Id: rs909687747

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.31893556G>C , CM000684.2:g.31893556G>C	GRCh38
NC_000022.10:g.32289542G>C , CM000684.1:g.32289542G>C	GRCh37
NC_000022.9:g.30619542G>C	NCBI36
NG_034067.1:g.144606G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382112.8:c.4034-26G>C	ENSP00000371546.4:n.4034-26G>C
ENST00000400246.7:c.3734-26G>C	ENSP00000383105.3:n.3734-26G>C
ENST00000400248.7:c.3941-26G>C	ENSP00000383107.1:n.3941-26G>C
ENST00000400249.7:c.3968-26G>C	ENSP00000383108.3:n.3968-26G>C
ENST00000433147.2:c.3950-26G>C	ENSP00000410544.2:n.3950-26G>C
ENST00000448753.6:c.1981-26G>C	ENSP00000402173.1:n.1981-26G>C
ENST00000479261.2:n.917-26G>C
ENST00000535622.6:c.3734-26G>C	ENSP00000440210.1:n.3734-26G>C
ENST00000642212.1:n.756-26G>C
ENST00000642684.1:c.*3656-26G>C	ENSP00000494554.1:n.*3656-26G>C
ENST00000642696.1:c.3941-26G>C	ENSP00000495917.1:n.3941-26G>C
ENST00000642771.1:c.*2045-26G>C	ENSP00000496278.1:n.*2045-26G>C
ENST00000642915.1:n.744-26G>C
ENST00000642956.1:n.774-26G>C
ENST00000643021.1:n.993-26G>C
ENST00000643097.1:n.965-26G>C
ENST00000643395.1:c.*1-26G>C	ENSP00000496630.1:n.*1-26G>C
ENST00000643751.2:c.*150-26G>C	ENSP00000495496.1:n.*150-26G>C
ENST00000644162.1:c.*2662-26G>C	ENSP00000495371.1:n.*2662-26G>C
ENST00000644331.1:c.3968-26G>C	ENSP00000494406.1:n.3968-26G>C
ENST00000644690.1:n.973-26G>C
ENST00000645407.1:c.3992-26G>C	ENSP00000496252.1:n.3992-26G>C
ENST00000645494.1:c.*2018-26G>C	ENSP00000495338.1:n.*2018-26G>C
ENST00000645547.1:c.837-26G>C	ENSP00000496023.1:n.837-26G>C
ENST00000645560.1:c.3800-26G>C	ENSP00000495544.1:n.3800-26G>C
ENST00000645711.1:c.4007-26G>C	ENSP00000493489.1:n.4007-26G>C
ENST00000645755.1:c.*2840-26G>C	ENSP00000495873.1:n.*2840-26G>C
ENST00000646135.1:n.1506-26G>C
ENST00000646383.1:n.876-26G>C
ENST00000646465.1:c.3800-26G>C	ENSP00000495655.1:n.3800-26G>C
ENST00000646515.1:c.*520-26G>C	ENSP00000494700.1:n.*520-26G>C
ENST00000646701.1:c.1787-62583G>C	ENSP00000496158.1:n.1787-62583G>C
ENST00000646830.1:n.899-26G>C
ENST00000646969.1:c.3800-26G>C	ENSP00000496724.1:n.3800-26G>C
ENST00000646998.1:c.*1-26G>C	ENSP00000494662.1:n.*1-26G>C
ENST00000647343.1:c.3950-26G>C	ENSP00000494879.1:n.3950-26G>C
ENST00000651528.2:c.4034-26G>C MANE Select	ENSP00000498382.1:n.4034-26G>C
ENST00000382111.6:c.4034-26G>C	ENSP00000371545.2:n.4034-26G>C
ENST00000382112.7:c.4007-26G>C	ENSP00000371546.3:n.4007-26G>C
ENST00000400246.5:c.4034-26G>C	ENSP00000383105.2:n.4034-26G>C
ENST00000400248.6:c.3941-26G>C	ENSP00000383107.1:n.3941-26G>C
ENST00000400249.6:c.3941-26G>C	ENSP00000383108.2:n.3941-26G>C
ENST00000433147.1:c.2160-26G>C
ENST00000448753.5:c.1981-26G>C	ENSP00000402173.1:n.1981-26G>C
ENST00000535622.5:c.3734-26G>C	ENSP00000440210.1:n.3734-26G>C
NM_001136029.2:c.4007-26G>C	NP_001129501.1:n.4007-26G>C
NM_001242896.1:c.4034-26G>C	NP_001229825.1:n.4034-26G>C
NM_001242897.1:c.3734-26G>C	NP_001229826.1:n.3734-26G>C
NM_014662.4:c.3941-26G>C	NP_055477.1:n.3941-26G>C
NR_110988.1:n.3827-26G>C
XM_005261862.1:c.4034-26G>C	XP_005261919.1:n.4034-26G>C
XM_011530557.1:c.4007-26G>C	XP_011528859.1:n.4007-26G>C
XM_011530558.1:c.3968-26G>C	XP_011528860.1:n.3968-26G>C
XM_011530559.1:c.3941-26G>C	XP_011528861.1:n.3941-26G>C
XM_011530560.1:c.3800-26G>C	XP_011528862.1:n.3800-26G>C
XM_011530561.1:c.3773-26G>C	XP_011528863.1:n.3773-26G>C
XM_011530562.1:c.4034-26G>C	XP_011528864.1:n.4034-26G>C
XM_011530563.1:c.3734-26G>C	XP_011528865.1:n.3734-26G>C
XM_011530564.1:c.4034-26G>C	XP_011528866.1:n.4034-26G>C
XM_011530565.1:c.*1-26G>C	XP_011528867.1:n.*1-26G>C
XM_011530569.1:c.1928-26G>C	XP_011528871.1:n.1928-26G>C
XR_937972.1:n.4301-26G>C
XR_937973.1:n.3888-26G>C
NM_001136029.3:c.4007-26G>C	NP_001129501.1:n.4007-26G>C
NM_001242896.2:c.4034-26G>C	NP_001229825.1:n.4034-26G>C
NM_001363852.1:c.3968-26G>C	NP_001350781.1:n.3968-26G>C
NM_001363854.1:c.3800-26G>C	NP_001350783.1:n.3800-26G>C
NM_001364318.1:c.4034-26G>C	NP_001351247.1:n.4034-26G>C
NM_001364319.1:c.3800-26G>C	NP_001351248.1:n.3800-26G>C
NM_001364320.1:c.3968-26G>C	NP_001351249.1:n.3968-26G>C
NM_014662.5:c.3941-26G>C	NP_055477.1:n.3941-26G>C
NR_110988.2:n.3831-26G>C
NR_146296.1:n.4223-26G>C
NR_157125.1:n.3931-26G>C
NR_157126.1:n.3803-26G>C
NR_157128.1:n.4065-26G>C
XM_011530557.2:c.4007-26G>C	XP_011528859.1:n.4007-26G>C
XM_011530559.2:c.3941-26G>C	XP_011528861.1:n.3941-26G>C
XM_011530561.2:c.3773-26G>C	XP_011528863.1:n.3773-26G>C
XM_011530562.2:c.4034-26G>C	XP_011528864.1:n.4034-26G>C
XM_011530563.2:c.3734-26G>C	XP_011528865.1:n.3734-26G>C
XM_011530565.2:c.*1-26G>C	XP_011528867.1:n.*1-26G>C
XM_011530569.2:c.1928-26G>C	XP_011528871.1:n.1928-26G>C
XM_024452305.1:c.1901-26G>C	XP_024308073.1:n.1901-26G>C
XR_001755389.1:n.4243-26G>C
XR_001755390.1:n.4313-26G>C
XR_937973.2:n.3900-26G>C
NM_001242896.3:c.4034-26G>C MANE Select	NP_001229825.1:n.4034-26G>C
NM_001242897.2:c.3734-26G>C	NP_001229826.1:n.3734-26G>C
NM_001363852.2:c.3968-26G>C	NP_001350781.1:n.3968-26G>C
NM_001363854.2:c.3800-26G>C	NP_001350783.1:n.3800-26G>C
NM_001369901.1:c.3950-26G>C	NP_001356830.1:n.3950-26G>C
NM_001369902.1:c.3950-26G>C	NP_001356831.1:n.3950-26G>C
NM_001369903.1:c.3941-26G>C	NP_001356832.1:n.3941-26G>C
NR_146296.2:n.4206-26G>C
NM_001136029.4:c.4007-26G>C	NP_001129501.1:n.4007-26G>C
NM_001364318.2:c.4034-26G>C	NP_001351247.1:n.4034-26G>C
NM_001364319.2:c.3800-26G>C	NP_001351248.1:n.3800-26G>C
NM_001364320.2:c.3968-26G>C	NP_001351249.1:n.3968-26G>C
NM_014662.6:c.3941-26G>C	NP_055477.1:n.3941-26G>C
NR_157125.2:n.3931-26G>C
NR_157126.2:n.3803-26G>C