Canonical Allele Identifier: CA402130785

Gene: DSG2

Linked Data

• dbSNP Id: rs121913006
• MyVariant Identifiers: chr18:g.29099830G>C (hg19) ; chr18:g.31519867G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31519867G>C , CM000680.2:g.31519867G>C	GRCh38
NC_000018.9:g.29099830G>C , CM000680.1:g.29099830G>C	GRCh37
NC_000018.8:g.27353828G>C	NCBI36
NG_007072.3:g.26626G>C , LRG_397:g.26626G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682241.2:c.146G>C	ENSP00000507600.2:p.Arg49Pro
ENST00000683654.1:c.146G>C	ENSP00000506971.1:p.Arg49Pro
ENST00000261590.13:c.146G>C MANE Select	ENSP00000261590.8:p.Arg49Pro
ENST00000261590.12:c.146G>C	ENSP00000261590.8:p.Arg49Pro
ENST00000585206.1:c.146G>C	ENSP00000462503.1:p.Arg49Pro
NM_001943.3:c.146G>C , LRG_397t1:c.146G>C	NP_001934.2:p.Arg49Pro
NM_001943.4:c.146G>C	NP_001934.2:p.Arg49Pro
XM_024451095.1:c.-389G>C	XP_024306863.1:n.-389G>C
NM_001943.5:c.146G>C MANE Select	NP_001934.2:p.Arg49Pro