Canonical Allele Identifier: CA402135380

Gene: DSG2

Linked Data

• MyVariant Identifiers: chr18:g.29104671A>T (hg19) ; chr18:g.31524708A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31524708A>T , CM000680.2:g.31524708A>T	GRCh38
NC_000018.9:g.29104671A>T , CM000680.1:g.29104671A>T	GRCh37
NC_000018.8:g.27358669A>T	NCBI36
NG_007072.3:g.31467A>T , LRG_397:g.31467A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682087.2:n.665A>T
ENST00000683614.2:n.665A>T
ENST00000682087.1:c.665A>T
ENST00000683614.1:c.665A>T
ENST00000261590.13:c.834A>T MANE Select	ENSP00000261590.8:p.Glu278Asp
ENST00000261590.12:c.834A>T	ENSP00000261590.8:p.Glu278Asp
NM_001943.3:c.834A>T , LRG_397t1:c.834A>T	NP_001934.2:p.Glu278Asp
NM_001943.4:c.834A>T	NP_001934.2:p.Glu278Asp
XM_024451095.1:c.300A>T	XP_024306863.1:p.Glu100Asp
NM_001943.5:c.834A>T MANE Select	NP_001934.2:p.Glu278Asp