Canonical Allele Identifier: CA2293861990

Gene: DSG2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31536375G= , CM000680.2:g.31536375G=	GRCh38
NC_000018.9:g.29116338G= , CM000680.1:g.29116338G=	GRCh37
NC_000018.8:g.27370336G=	NCBI36
NG_007072.3:g.43134G= , LRG_397:g.43134G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261590.13:c.1597G= MANE Select	ENSP00000261590.8:p.Val533=
ENST00000261590.12:c.1597G=	ENSP00000261590.8:p.Val533=
NM_001943.3:c.1597G= , LRG_397t1:c.1597G=	NP_001934.2:p.Val533=
NM_001943.4:c.1597G=	NP_001934.2:p.Val533=
XM_024451095.1:c.1063G=	XP_024306863.1:p.Val355=
NM_001943.5:c.1597G= MANE Select	NP_001934.2:p.Val533=