Canonical Allele Identifier: CA2293859920

Gene: DSG2

Linked Data

• dbSNP Id: rs1259592674

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31531437A>T , CM000680.2:g.31531437A>T	GRCh38
NC_000018.9:g.29111400A>T , CM000680.1:g.29111400A>T	GRCh37
NC_000018.8:g.27365398A>T	NCBI36
NG_007072.3:g.38196A>T , LRG_397:g.38196A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683614.2:n.1296A>T
ENST00000683614.1:c.1296A>T
ENST00000261590.13:c.1280+185A>T MANE Select	ENSP00000261590.8:n.1280+185A>T
ENST00000261590.12:c.1280+185A>T	ENSP00000261590.8:n.1280+185A>T
NM_001943.3:c.1280+185A>T , LRG_397t1:c.1280+185A>T	NP_001934.2:n.1280+185A>T
NM_001943.4:c.1280+185A>T	NP_001934.2:n.1280+185A>T
XM_024451095.1:c.746+185A>T	XP_024306863.1:n.746+185A>T
NM_001943.5:c.1280+185A>T MANE Select	NP_001934.2:n.1280+185A>T