Canonical Allele Identifier: CA2293855019

Gene: DSG2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31519937G= , CM000680.2:g.31519937G=	GRCh38
NC_000018.9:g.29099900G= , CM000680.1:g.29099900G=	GRCh37
NC_000018.8:g.27353898G=	NCBI36
NG_007072.3:g.26696G= , LRG_397:g.26696G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682087.2:n.47G=
ENST00000682241.2:c.216G=	ENSP00000507600.2:p.Lys72=
ENST00000683614.2:n.47G=
ENST00000682087.1:c.47G=
ENST00000682241.1:c.47G=
ENST00000683614.1:c.47G=
ENST00000683654.1:c.216G=	ENSP00000506971.1:p.Lys72=
ENST00000684461.1:n.47G=
ENST00000261590.13:c.216G= MANE Select	ENSP00000261590.8:p.Lys72=
ENST00000261590.12:c.216G=	ENSP00000261590.8:p.Lys72=
ENST00000585206.1:c.216G=	ENSP00000462503.1:p.Lys72=
NM_001943.3:c.216G= , LRG_397t1:c.216G=	NP_001934.2:p.Lys72=
NM_001943.4:c.216G=	NP_001934.2:p.Lys72=
XM_024451095.1:c.-319G=	XP_024306863.1:n.-319G=
NM_001943.5:c.216G= MANE Select	NP_001934.2:p.Lys72=