Canonical Allele Identifier: CA402133599

Gene: DSG2

Linked Data

• MyVariant Identifiers: chr18:g.29102111T>G (hg19) ; chr18:g.31522148T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31522148T>G , CM000680.2:g.31522148T>G	GRCh38
NC_000018.9:g.29102111T>G , CM000680.1:g.29102111T>G	GRCh37
NC_000018.8:g.27356109T>G	NCBI36
NG_007072.3:g.28907T>G , LRG_397:g.28907T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682087.2:n.420T>G
ENST00000682241.2:c.589T>G	ENSP00000507600.2:p.Ser197Ala
ENST00000683614.2:n.420T>G
ENST00000682087.1:c.420T>G
ENST00000682241.1:c.420T>G
ENST00000683614.1:c.420T>G
ENST00000683654.1:c.589T>G	ENSP00000506971.1:p.Ser197Ala
ENST00000684461.1:n.1259T>G
ENST00000261590.13:c.589T>G MANE Select	ENSP00000261590.8:p.Ser197Ala
ENST00000261590.12:c.589T>G	ENSP00000261590.8:p.Ser197Ala
ENST00000585206.1:c.589T>G	ENSP00000462503.1:p.Ser197Ala
NM_001943.3:c.589T>G , LRG_397t1:c.589T>G	NP_001934.2:p.Ser197Ala
NM_001943.4:c.589T>G	NP_001934.2:p.Ser197Ala
XM_024451095.1:c.55T>G	XP_024306863.1:p.Ser19Ala
NM_001943.5:c.589T>G MANE Select	NP_001934.2:p.Ser197Ala