Canonical Allele Identifier: CA2293855899

Gene: DSG2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31522209C= , CM000680.2:g.31522209C=	GRCh38
NC_000018.9:g.29102172C= , CM000680.1:g.29102172C=	GRCh37
NC_000018.8:g.27356170C=	NCBI36
NG_007072.3:g.28968C= , LRG_397:g.28968C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682087.2:n.481C=
ENST00000682241.2:c.650C=	ENSP00000507600.2:p.Thr217=
ENST00000683614.2:n.481C=
ENST00000682087.1:c.481C=
ENST00000682241.1:c.481C=
ENST00000683614.1:c.481C=
ENST00000683654.1:c.650C=	ENSP00000506971.1:p.Thr217=
ENST00000684461.1:n.1320C=
ENST00000261590.13:c.650C= MANE Select	ENSP00000261590.8:p.Thr217=
ENST00000261590.12:c.650C=	ENSP00000261590.8:p.Thr217=
ENST00000585206.1:c.650C=	ENSP00000462503.1:p.Thr217=
NM_001943.3:c.650C= , LRG_397t1:c.650C=	NP_001934.2:p.Thr217=
NM_001943.4:c.650C=	NP_001934.2:p.Thr217=
XM_024451095.1:c.116C=	XP_024306863.1:p.Thr39=
NM_001943.5:c.650C= MANE Select	NP_001934.2:p.Thr217=