Canonical Allele Identifier: CA503597234

Gene: DSG2

Linked Data

• ClinVar Variation Id: 1576337
• ClinVar RCV Id: RCV002078309 ; RCV004005330
• dbSNP Id: rs935833101
• MyVariant Identifiers: chr18:g.29101127G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31521164G>A , CM000680.2:g.31521164G>A	GRCh38
NC_000018.9:g.29101127G>A , CM000680.1:g.29101127G>A	GRCh37
NC_000018.8:g.27355125G>A	NCBI36
NG_007072.3:g.27923G>A , LRG_397:g.27923G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682087.2:n.275G>A
ENST00000682241.2:c.444G>A	ENSP00000507600.2:p.Lys148=
ENST00000683614.2:n.275G>A
ENST00000682087.1:c.275G>A
ENST00000682241.1:c.275G>A
ENST00000683614.1:c.275G>A
ENST00000683654.1:c.444G>A	ENSP00000506971.1:p.Lys148=
ENST00000684461.1:n.275G>A
ENST00000261590.13:c.444G>A MANE Select	ENSP00000261590.8:p.Lys148=
ENST00000261590.12:c.444G>A	ENSP00000261590.8:p.Lys148=
ENST00000585206.1:c.444G>A	ENSP00000462503.1:p.Lys148=
NM_001943.3:c.444G>A , LRG_397t1:c.444G>A	NP_001934.2:p.Lys148=
NM_001943.4:c.444G>A	NP_001934.2:p.Lys148=
XM_024451095.1:c.-91G>A	XP_024306863.1:n.-91G>A
NM_001943.5:c.444G>A MANE Select	NP_001934.2:p.Lys148=