Canonical Allele Identifier: CA402137937
Gene: DSG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 452787
dbSNP Id: rs1555627108

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31530999G>T , CM000680.2:g.31530999G>T GRCh38
NC_000018.9:g.29110962G>T , CM000680.1:g.29110962G>T GRCh37
NC_000018.8:g.27364960G>T NCBI36
NG_007072.3:g.37758G>T , LRG_397:g.37758G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000683614.2:n.858G>T
ENST00000683614.1:c.858G>T
ENST00000261590.13:c.1027G>T MANE Select ENSP00000261590.8:p.Glu343Ter
ENST00000261590.12:c.1027G>T ENSP00000261590.8:p.Glu343Ter
NM_001943.3:c.1027G>T , LRG_397t1:c.1027G>T NP_001934.2:p.Glu343Ter
NM_001943.4:c.1027G>T NP_001934.2:p.Glu343Ter
XM_024451095.1:c.493G>T XP_024306863.1:p.Glu165Ter
NM_001943.5:c.1027G>T MANE Select NP_001934.2:p.Glu343Ter