Canonical Allele Identifier: CA2293855856

Gene: DSG2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31522126C= , CM000680.2:g.31522126C=	GRCh38
NC_000018.9:g.29102089C= , CM000680.1:g.29102089C=	GRCh37
NC_000018.8:g.27356087C=	NCBI36
NG_007072.3:g.28885C= , LRG_397:g.28885C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682087.2:n.398C=
ENST00000682241.2:c.567C=	ENSP00000507600.2:p.Pro189=
ENST00000683614.2:n.398C=
ENST00000682087.1:c.398C=
ENST00000682241.1:c.398C=
ENST00000683614.1:c.398C=
ENST00000683654.1:c.567C=	ENSP00000506971.1:p.Pro189=
ENST00000684461.1:n.1237C=
ENST00000261590.13:c.567C= MANE Select	ENSP00000261590.8:p.Pro189=
ENST00000261590.12:c.567C=	ENSP00000261590.8:p.Pro189=
ENST00000585206.1:c.567C=	ENSP00000462503.1:p.Pro189=
NM_001943.3:c.567C= , LRG_397t1:c.567C=	NP_001934.2:p.Pro189=
NM_001943.4:c.567C=	NP_001934.2:p.Pro189=
XM_024451095.1:c.33C=	XP_024306863.1:p.Pro11=
NM_001943.5:c.567C= MANE Select	NP_001934.2:p.Pro189=