Canonical Allele Identifier: CA402133683

Gene: DSG2

Linked Data

• ClinVar Variation Id: 927518
• ClinVar RCV Id: RCV001190832
• dbSNP Id: rs2073131985
• COSMIC: COSM987620
• MyVariant Identifiers: chr18:g.29102127C>A (hg19) ; chr18:g.31522164C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31522164C>A , CM000680.2:g.31522164C>A	GRCh38
NC_000018.9:g.29102127C>A , CM000680.1:g.29102127C>A	GRCh37
NC_000018.8:g.27356125C>A	NCBI36
NG_007072.3:g.28923C>A , LRG_397:g.28923C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682087.2:n.436C>A
ENST00000682241.2:c.605C>A	ENSP00000507600.2:p.Ser202Tyr
ENST00000683614.2:n.436C>A
ENST00000682087.1:c.436C>A
ENST00000682241.1:c.436C>A
ENST00000683614.1:c.436C>A
ENST00000683654.1:c.605C>A	ENSP00000506971.1:p.Ser202Tyr
ENST00000684461.1:n.1275C>A
ENST00000261590.13:c.605C>A MANE Select	ENSP00000261590.8:p.Ser202Tyr
ENST00000261590.12:c.605C>A	ENSP00000261590.8:p.Ser202Tyr
ENST00000585206.1:c.605C>A	ENSP00000462503.1:p.Ser202Tyr
NM_001943.3:c.605C>A , LRG_397t1:c.605C>A	NP_001934.2:p.Ser202Tyr
NM_001943.4:c.605C>A	NP_001934.2:p.Ser202Tyr
XM_024451095.1:c.71C>A	XP_024306863.1:p.Ser24Tyr
NM_001943.5:c.605C>A MANE Select	NP_001934.2:p.Ser202Tyr