Canonical Allele Identifier: CA411294499
Gene: DEPDC5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.32257355A>C (hg19) chr22:g.31861369A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.31861369A>C , CM000684.2:g.31861369A>C GRCh38
NC_000022.10:g.32257355A>C , CM000684.1:g.32257355A>C GRCh37
NC_000022.9:g.30587355A>C NCBI36
NG_034067.1:g.112419A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000382112.8:c.3266A>C ENSP00000371546.4:p.Asp1089Ala
ENST00000400246.7:c.3030+3816A>C ENSP00000383105.3:n.3030+3816A>C
ENST00000400248.7:c.3237+3816A>C ENSP00000383107.1:n.3237+3816A>C
ENST00000400249.7:c.3264+3816A>C ENSP00000383108.3:n.3264+3816A>C
ENST00000433147.2:c.3182A>C ENSP00000410544.2:p.Asp1061Ala
ENST00000448753.6:c.1322A>C ENSP00000402173.1:p.Asp441Ala
ENST00000535622.6:c.3030+3816A>C ENSP00000440210.1:n.3030+3816A>C
ENST00000642684.1:c.*2957+3816A>C ENSP00000494554.1:n.*2957+3816A>C
ENST00000642696.1:c.3237+3816A>C ENSP00000495917.1:n.3237+3816A>C
ENST00000642771.1:c.*1277A>C ENSP00000496278.1:n.*1277A>C
ENST00000642956.1:n.6A>C
ENST00000643021.1:n.289+3816A>C
ENST00000643097.1:n.197A>C
ENST00000643395.1:c.3030+3816A>C ENSP00000496630.1:n.3030+3816A>C
ENST00000643751.2:c.3266A>C ENSP00000495496.1:p.Asp1089Ala
ENST00000644162.1:c.*1894A>C ENSP00000495371.1:n.*1894A>C
ENST00000644331.1:c.3264+3816A>C ENSP00000494406.1:n.3264+3816A>C
ENST00000644690.1:n.186+3816A>C
ENST00000645407.1:c.3288+3816A>C ENSP00000496252.1:n.3288+3816A>C
ENST00000645494.1:c.*1250A>C ENSP00000495338.1:n.*1250A>C
ENST00000645560.1:c.3032A>C ENSP00000495544.1:p.Asp1011Ala
ENST00000645711.1:c.3239A>C ENSP00000493489.1:p.Asp1080Ala
ENST00000645755.1:c.*2136+3816A>C ENSP00000495873.1:n.*2136+3816A>C
ENST00000645893.1:n.2123A>C
ENST00000646135.1:n.738A>C
ENST00000646465.1:c.3032A>C ENSP00000495655.1:p.Asp1011Ala
ENST00000646515.1:c.3266A>C ENSP00000494700.1:p.Asp1089Ala
ENST00000646701.1:c.1786+42144A>C ENSP00000496158.1:n.1786+42144A>C
ENST00000646830.1:n.195+3816A>C
ENST00000646969.1:c.3032A>C ENSP00000496724.1:p.Asp1011Ala
ENST00000646998.1:c.3264+3816A>C ENSP00000494662.1:n.3264+3816A>C
ENST00000647343.1:c.3182A>C ENSP00000494879.1:p.Asp1061Ala
ENST00000651528.2:c.3266A>C MANE Select ENSP00000498382.1:p.Asp1089Ala
ENST00000382111.6:c.3266A>C ENSP00000371545.2:p.Asp1089Ala
ENST00000382112.7:c.3239A>C ENSP00000371546.3:p.Asp1080Ala
ENST00000400246.5:c.3266A>C ENSP00000383105.2:p.Asp1089Ala
ENST00000400248.6:c.3237+3816A>C ENSP00000383107.1:n.3237+3816A>C
ENST00000400249.6:c.3237+3816A>C ENSP00000383108.2:n.3237+3816A>C
ENST00000433147.1:c.1456+3816A>C
ENST00000448753.5:c.1322A>C ENSP00000402173.1:p.Asp441Ala
ENST00000494060.1:n.138+3816A>C
ENST00000535622.5:c.3030+3816A>C ENSP00000440210.1:n.3030+3816A>C
NM_001136029.2:c.3239A>C NP_001129501.1:p.Asp1080Ala
NM_001242896.1:c.3266A>C NP_001229825.1:p.Asp1089Ala
NM_001242897.1:c.3030+3816A>C NP_001229826.1:n.3030+3816A>C
NM_014662.4:c.3237+3816A>C NP_055477.1:n.3237+3816A>C
NR_110988.1:n.3232+3816A>C
XM_005261862.1:c.3266A>C XP_005261919.1:p.Asp1089Ala
XM_011530557.1:c.3239A>C XP_011528859.1:p.Asp1080Ala
XM_011530558.1:c.3264+3816A>C XP_011528860.1:n.3264+3816A>C
XM_011530559.1:c.3237+3816A>C XP_011528861.1:n.3237+3816A>C
XM_011530560.1:c.3032A>C XP_011528862.1:p.Asp1011Ala
XM_011530561.1:c.3005A>C XP_011528863.1:p.Asp1002Ala
XM_011530562.1:c.3266A>C XP_011528864.1:p.Asp1089Ala
XM_011530563.1:c.3030+3816A>C XP_011528865.1:n.3030+3816A>C
XM_011530564.1:c.3266A>C XP_011528866.1:p.Asp1089Ala
XM_011530565.1:c.3266A>C XP_011528867.1:p.Asp1089Ala
XM_011530566.1:c.3266A>C XP_011528868.1:p.Asp1089Ala
XM_011530567.1:c.3266A>C XP_011528869.1:p.Asp1089Ala
XM_011530568.1:c.3264+3816A>C XP_011528870.1:n.3264+3816A>C
XM_011530569.1:c.1160A>C XP_011528871.1:p.Asp387Ala
XR_937972.1:n.3463A>C
XR_937973.1:n.3229A>C
NM_001136029.3:c.3239A>C NP_001129501.1:p.Asp1080Ala
NM_001242896.2:c.3266A>C NP_001229825.1:p.Asp1089Ala
NM_001363852.1:c.3264+3816A>C NP_001350781.1:n.3264+3816A>C
NM_001363854.1:c.3032A>C NP_001350783.1:p.Asp1011Ala
NM_001364318.1:c.3266A>C NP_001351247.1:p.Asp1089Ala
NM_001364319.1:c.3032A>C NP_001351248.1:p.Asp1011Ala
NM_001364320.1:c.3264+3816A>C NP_001351249.1:n.3264+3816A>C
NM_014662.5:c.3237+3816A>C NP_055477.1:n.3237+3816A>C
NR_110988.2:n.3236+3816A>C
NR_146296.1:n.3372A>C
NR_157125.1:n.3227+3816A>C
NR_157126.1:n.3355A>C
NR_157128.1:n.3470+3816A>C
XM_011530557.2:c.3239A>C XP_011528859.1:p.Asp1080Ala
XM_011530559.2:c.3237+3816A>C XP_011528861.1:n.3237+3816A>C
XM_011530561.2:c.3005A>C XP_011528863.1:p.Asp1002Ala
XM_011530562.2:c.3266A>C XP_011528864.1:p.Asp1089Ala
XM_011530563.2:c.3030+3816A>C XP_011528865.1:n.3030+3816A>C
XM_011530565.2:c.3266A>C XP_011528867.1:p.Asp1089Ala
XM_011530568.2:c.3264+3816A>C XP_011528870.1:n.3264+3816A>C
XM_011530569.2:c.1160A>C XP_011528871.1:p.Asp387Ala
XM_024452305.1:c.1133A>C XP_024308073.1:p.Asp378Ala
XR_001755389.1:n.3475A>C
XR_001755390.1:n.3475A>C
XR_937973.2:n.3241A>C
NM_001242896.3:c.3266A>C MANE Select NP_001229825.1:p.Asp1089Ala
NM_001242897.2:c.3030+3816A>C NP_001229826.1:n.3030+3816A>C
NM_001363852.2:c.3264+3816A>C NP_001350781.1:n.3264+3816A>C
NM_001363854.2:c.3032A>C NP_001350783.1:p.Asp1011Ala
NM_001369901.1:c.3182A>C NP_001356830.1:p.Asp1061Ala
NM_001369902.1:c.3182A>C NP_001356831.1:p.Asp1061Ala
NM_001369903.1:c.3237+3816A>C NP_001356832.1:n.3237+3816A>C
NR_146296.2:n.3355A>C
NM_001136029.4:c.3239A>C NP_001129501.1:p.Asp1080Ala
NM_001364318.2:c.3266A>C NP_001351247.1:p.Asp1089Ala
NM_001364319.2:c.3032A>C NP_001351248.1:p.Asp1011Ala
NM_001364320.2:c.3264+3816A>C NP_001351249.1:n.3264+3816A>C
NM_014662.6:c.3237+3816A>C NP_055477.1:n.3237+3816A>C
NR_157125.2:n.3227+3816A>C
NR_157126.2:n.3355A>C
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