Canonical Allele Identifier: CA402135214

Gene: DSG2

Linked Data

• MyVariant Identifiers: chr18:g.29104520A>T (hg19) ; chr18:g.31524557A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31524557A>T , CM000680.2:g.31524557A>T	GRCh38
NC_000018.9:g.29104520A>T , CM000680.1:g.29104520A>T	GRCh37
NC_000018.8:g.27358518A>T	NCBI36
NG_007072.3:g.31316A>T , LRG_397:g.31316A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682087.2:n.631A>T
ENST00000683614.2:n.631A>T
ENST00000682087.1:c.631A>T
ENST00000683614.1:c.631A>T
ENST00000261590.13:c.800A>T MANE Select	ENSP00000261590.8:p.Asp267Val
ENST00000261590.12:c.800A>T	ENSP00000261590.8:p.Asp267Val
NM_001943.3:c.800A>T , LRG_397t1:c.800A>T	NP_001934.2:p.Asp267Val
NM_001943.4:c.800A>T	NP_001934.2:p.Asp267Val
XM_024451095.1:c.266A>T	XP_024306863.1:p.Asp89Val
NM_001943.5:c.800A>T MANE Select	NP_001934.2:p.Asp267Val