Canonical Allele Identifier: CA2293855862

Gene: DSG2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31522139T= , CM000680.2:g.31522139T=	GRCh38
NC_000018.9:g.29102102T= , CM000680.1:g.29102102T=	GRCh37
NC_000018.8:g.27356100T=	NCBI36
NG_007072.3:g.28898T= , LRG_397:g.28898T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682087.2:n.411T=
ENST00000682241.2:c.580T=	ENSP00000507600.2:p.Ser194=
ENST00000683614.2:n.411T=
ENST00000682087.1:c.411T=
ENST00000682241.1:c.411T=
ENST00000683614.1:c.411T=
ENST00000683654.1:c.580T=	ENSP00000506971.1:p.Ser194=
ENST00000684461.1:n.1250T=
ENST00000261590.13:c.580T= MANE Select	ENSP00000261590.8:p.Ser194=
ENST00000261590.12:c.580T=	ENSP00000261590.8:p.Ser194=
ENST00000585206.1:c.580T=	ENSP00000462503.1:p.Ser194=
NM_001943.3:c.580T= , LRG_397t1:c.580T=	NP_001934.2:p.Ser194=
NM_001943.4:c.580T=	NP_001934.2:p.Ser194=
XM_024451095.1:c.46T=	XP_024306863.1:p.Ser16=
NM_001943.5:c.580T= MANE Select	NP_001934.2:p.Ser194=