Canonical Allele Identifier: CA402135372

Gene: DSG2

Linked Data

• MyVariant Identifiers: chr18:g.29104669G>T (hg19) ; chr18:g.31524706G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31524706G>T , CM000680.2:g.31524706G>T	GRCh38
NC_000018.9:g.29104669G>T , CM000680.1:g.29104669G>T	GRCh37
NC_000018.8:g.27358667G>T	NCBI36
NG_007072.3:g.31465G>T , LRG_397:g.31465G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682087.2:n.663G>T
ENST00000683614.2:n.663G>T
ENST00000682087.1:c.663G>T
ENST00000683614.1:c.663G>T
ENST00000261590.13:c.832G>T MANE Select	ENSP00000261590.8:p.Glu278Ter
ENST00000261590.12:c.832G>T	ENSP00000261590.8:p.Glu278Ter
NM_001943.3:c.832G>T , LRG_397t1:c.832G>T	NP_001934.2:p.Glu278Ter
NM_001943.4:c.832G>T	NP_001934.2:p.Glu278Ter
XM_024451095.1:c.298G>T	XP_024306863.1:p.Glu100Ter
NM_001943.5:c.832G>T MANE Select	NP_001934.2:p.Glu278Ter