Canonical Allele Identifier: CA2293861930

Gene: DSG2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31536236T= , CM000680.2:g.31536236T=	GRCh38
NC_000018.9:g.29116199T= , CM000680.1:g.29116199T=	GRCh37
NC_000018.8:g.27370197T=	NCBI36
NG_007072.3:g.42995T= , LRG_397:g.42995T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261590.13:c.1458T= MANE Select	ENSP00000261590.8:p.Leu486=
ENST00000261590.12:c.1458T=	ENSP00000261590.8:p.Leu486=
NM_001943.3:c.1458T= , LRG_397t1:c.1458T=	NP_001934.2:p.Leu486=
NM_001943.4:c.1458T=	NP_001934.2:p.Leu486=
XM_024451095.1:c.924T=	XP_024306863.1:p.Leu308=
NM_001943.5:c.1458T= MANE Select	NP_001934.2:p.Leu486=