Canonical Allele Identifier: CA2293861932

Gene: DSG2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31536241A= , CM000680.2:g.31536241A=	GRCh38
NC_000018.9:g.29116204A= , CM000680.1:g.29116204A=	GRCh37
NC_000018.8:g.27370202A=	NCBI36
NG_007072.3:g.43000A= , LRG_397:g.43000A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261590.13:c.1463A= MANE Select	ENSP00000261590.8:p.Asn488=
ENST00000261590.12:c.1463A=	ENSP00000261590.8:p.Asn488=
NM_001943.3:c.1463A= , LRG_397t1:c.1463A=	NP_001934.2:p.Asn488=
NM_001943.4:c.1463A=	NP_001934.2:p.Asn488=
XM_024451095.1:c.929A=	XP_024306863.1:p.Asn310=
NM_001943.5:c.1463A= MANE Select	NP_001934.2:p.Asn488=