Canonical Allele Identifier: CA402131599

Gene: DSG2

Linked Data

• MyVariant Identifiers: chr18:g.29100885T>A (hg19) ; chr18:g.31520922T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31520922T>A , CM000680.2:g.31520922T>A	GRCh38
NC_000018.9:g.29100885T>A , CM000680.1:g.29100885T>A	GRCh37
NC_000018.8:g.27354883T>A	NCBI36
NG_007072.3:g.27681T>A , LRG_397:g.27681T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682087.2:n.167T>A
ENST00000682241.2:c.336T>A	ENSP00000507600.2:p.Asn112Lys
ENST00000683614.2:n.167T>A
ENST00000682087.1:c.167T>A
ENST00000682241.1:c.167T>A
ENST00000683614.1:c.167T>A
ENST00000683654.1:c.336T>A	ENSP00000506971.1:p.Asn112Lys
ENST00000684461.1:n.167T>A
ENST00000261590.13:c.336T>A MANE Select	ENSP00000261590.8:p.Asn112Lys
ENST00000261590.12:c.336T>A	ENSP00000261590.8:p.Asn112Lys
ENST00000585206.1:c.336T>A	ENSP00000462503.1:p.Asn112Lys
NM_001943.3:c.336T>A , LRG_397t1:c.336T>A	NP_001934.2:p.Asn112Lys
NM_001943.4:c.336T>A	NP_001934.2:p.Asn112Lys
XM_024451095.1:c.-199T>A	XP_024306863.1:n.-199T>A
NM_001943.5:c.336T>A MANE Select	NP_001934.2:p.Asn112Lys