Canonical Allele Identifier: CA1608620567

Gene: DSP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7567366_7567368delinsACT , CM000668.2:g.7567366_7567368delinsACT	GRCh38
NC_000006.11:g.7567599_7567601delinsACT , CM000668.1:g.7567599_7567601delinsACT	GRCh37
NC_000006.10:g.7512598_7512600delinsACT	NCBI36
NG_008803.1:g.30730_30732delinsACT , LRG_423:g.30730_30732delinsACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.1057_1059delinsACT	ENSP00000518230.1:p.Thr353=
ENST00000682228.1:n.381_383delinsACT
ENST00000379802.8:c.1057_1059delinsACT MANE Select	ENSP00000369129.3:p.Thr353=
ENST00000379802.7:c.1057_1059delinsACT	ENSP00000369129.3:p.Thr353=
ENST00000418664.2:c.1057_1059delinsACT	ENSP00000396591.2:p.Thr353=
NM_001008844.1:c.1057_1059delinsACT	NP_001008844.1:p.Thr353=
NM_004415.2:c.1057_1059delinsACT , LRG_423t1:c.1057_1059delinsACT	NP_004406.2:p.Thr353=
XM_011514323.1:c.1057_1059delinsACT	XP_011512625.1:p.Thr353=
NM_001008844.2:c.1057_1059delinsACT	NP_001008844.1:p.Thr353=
NM_001319034.1:c.1057_1059delinsACT	NP_001305963.1:p.Thr353=
NM_004415.3:c.1057_1059delinsACT	NP_004406.2:p.Thr353=
NM_004415.4:c.1057_1059delinsACT MANE Select	NP_004406.2:p.Thr353=
NM_001008844.3:c.1057_1059delinsACT	NP_001008844.1:p.Thr353=
NM_001319034.2:c.1057_1059delinsACT	NP_001305963.1:p.Thr353=