Canonical Allele Identifier: CA402139311

Gene: DSG2

Linked Data

• MyVariant Identifiers: chr18:g.29111157C>T (hg19) ; chr18:g.31531194C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31531194C>T , CM000680.2:g.31531194C>T	GRCh38
NC_000018.9:g.29111157C>T , CM000680.1:g.29111157C>T	GRCh37
NC_000018.8:g.27365155C>T	NCBI36
NG_007072.3:g.37953C>T , LRG_397:g.37953C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000683614.2:n.1053C>T
ENST00000683614.1:c.1053C>T
ENST00000261590.13:c.1222C>T MANE Select	ENSP00000261590.8:p.Gln408Ter
ENST00000261590.12:c.1222C>T	ENSP00000261590.8:p.Gln408Ter
NM_001943.3:c.1222C>T , LRG_397t1:c.1222C>T	NP_001934.2:p.Gln408Ter
NM_001943.4:c.1222C>T	NP_001934.2:p.Gln408Ter
XM_024451095.1:c.688C>T	XP_024306863.1:p.Gln230Ter
NM_001943.5:c.1222C>T MANE Select	NP_001934.2:p.Gln408Ter