Canonical Allele Identifier: CA2677235480

Gene: DSP

Linked Data

• gnomAD v4: 6-7583393-CCA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7583396_7583397del , CM000668.2:g.7583396_7583397del	GRCh38
NC_000006.11:g.7583629_7583630del , CM000668.1:g.7583629_7583630del	GRCh37
NC_000006.10:g.7528628_7528629del	NCBI36
NG_008803.1:g.46760_46761del , LRG_423:g.46760_46761del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.4805_4806del	ENSP00000518230.1:p.Thr1602SerfsTer15
ENST00000379802.8:c.6134_6135del MANE Select	ENSP00000369129.3:p.Thr2045SerfsTer15
ENST00000379802.7:c.6134_6135del	ENSP00000369129.3:p.Thr2045SerfsTer15
ENST00000418664.2:c.4337_4338del	ENSP00000396591.2:p.Thr1446SerfsTer15
NM_001008844.1:c.4337_4338del	NP_001008844.1:p.Thr1446SerfsTer15
NM_004415.2:c.6134_6135del , LRG_423t1:c.6134_6135del	NP_004406.2:p.Thr2045SerfsTer15
XM_011514323.1:c.4805_4806del	XP_011512625.1:p.Thr1602SerfsTer15
NM_001008844.2:c.4337_4338del	NP_001008844.1:p.Thr1446SerfsTer15
NM_001319034.1:c.4805_4806del	NP_001305963.1:p.Thr1602SerfsTer15
NM_004415.3:c.6134_6135del	NP_004406.2:p.Thr2045SerfsTer15
NM_004415.4:c.6134_6135del MANE Select	NP_004406.2:p.Thr2045SerfsTer15
NM_001008844.3:c.4337_4338del	NP_001008844.1:p.Thr1446SerfsTer15
NM_001319034.2:c.4805_4806del	NP_001305963.1:p.Thr1602SerfsTer15