Canonical Allele Identifier: CA402133603

Gene: DSG2

Linked Data

• COSMIC: COSM3525244
• MyVariant Identifiers: chr18:g.29102112C>T (hg19) ; chr18:g.31522149C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31522149C>T , CM000680.2:g.31522149C>T	GRCh38
NC_000018.9:g.29102112C>T , CM000680.1:g.29102112C>T	GRCh37
NC_000018.8:g.27356110C>T	NCBI36
NG_007072.3:g.28908C>T , LRG_397:g.28908C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682087.2:n.421C>T
ENST00000682241.2:c.590C>T	ENSP00000507600.2:p.Ser197Phe
ENST00000683614.2:n.421C>T
ENST00000682087.1:c.421C>T
ENST00000682241.1:c.421C>T
ENST00000683614.1:c.421C>T
ENST00000683654.1:c.590C>T	ENSP00000506971.1:p.Ser197Phe
ENST00000684461.1:n.1260C>T
ENST00000261590.13:c.590C>T MANE Select	ENSP00000261590.8:p.Ser197Phe
ENST00000261590.12:c.590C>T	ENSP00000261590.8:p.Ser197Phe
ENST00000585206.1:c.590C>T	ENSP00000462503.1:p.Ser197Phe
NM_001943.3:c.590C>T , LRG_397t1:c.590C>T	NP_001934.2:p.Ser197Phe
NM_001943.4:c.590C>T	NP_001934.2:p.Ser197Phe
XM_024451095.1:c.56C>T	XP_024306863.1:p.Ser19Phe
NM_001943.5:c.590C>T MANE Select	NP_001934.2:p.Ser197Phe