Canonical Allele Identifier: CA2293855878

Gene: DSG2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31522169G= , CM000680.2:g.31522169G=	GRCh38
NC_000018.9:g.29102132G= , CM000680.1:g.29102132G=	GRCh37
NC_000018.8:g.27356130G=	NCBI36
NG_007072.3:g.28928G= , LRG_397:g.28928G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682087.2:n.441G=
ENST00000682241.2:c.610G=	ENSP00000507600.2:p.Glu204=
ENST00000683614.2:n.441G=
ENST00000682087.1:c.441G=
ENST00000682241.1:c.441G=
ENST00000683614.1:c.441G=
ENST00000683654.1:c.610G=	ENSP00000506971.1:p.Glu204=
ENST00000684461.1:n.1280G=
ENST00000261590.13:c.610G= MANE Select	ENSP00000261590.8:p.Glu204=
ENST00000261590.12:c.610G=	ENSP00000261590.8:p.Glu204=
ENST00000585206.1:c.610G=	ENSP00000462503.1:p.Glu204=
NM_001943.3:c.610G= , LRG_397t1:c.610G=	NP_001934.2:p.Glu204=
NM_001943.4:c.610G=	NP_001934.2:p.Glu204=
XM_024451095.1:c.76G=	XP_024306863.1:p.Glu26=
NM_001943.5:c.610G= MANE Select	NP_001934.2:p.Glu204=