Canonical Allele Identifier: CA2293855407

Gene: DSG2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31521028T= , CM000680.2:g.31521028T=	GRCh38
NC_000018.9:g.29100991T= , CM000680.1:g.29100991T=	GRCh37
NC_000018.8:g.27354989T=	NCBI36
NG_007072.3:g.27787T= , LRG_397:g.27787T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682087.2:n.209+64T=
ENST00000682241.2:c.378+64T=	ENSP00000507600.2:n.378+64T=
ENST00000683614.2:n.209+64T=
ENST00000682087.1:c.209+64T=
ENST00000682241.1:c.209+64T=
ENST00000683614.1:c.209+64T=
ENST00000683654.1:c.378+64T=	ENSP00000506971.1:n.378+64T=
ENST00000684461.1:n.209+64T=
ENST00000261590.13:c.378+64T= MANE Select	ENSP00000261590.8:n.378+64T=
ENST00000261590.12:c.378+64T=	ENSP00000261590.8:n.378+64T=
ENST00000585206.1:c.378+64T=	ENSP00000462503.1:n.378+64T=
NM_001943.3:c.378+64T= , LRG_397t1:c.378+64T=	NP_001934.2:n.378+64T=
NM_001943.4:c.378+64T=	NP_001934.2:n.378+64T=
XM_024451095.1:c.-157+64T=	XP_024306863.1:n.-157+64T=
NM_001943.5:c.378+64T= MANE Select	NP_001934.2:n.378+64T=