Canonical Allele Identifier: CA402133780

Gene: DSG2

Linked Data

• MyVariant Identifiers: chr18:g.29102147C>A (hg19) ; chr18:g.31522184C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31522184C>A , CM000680.2:g.31522184C>A	GRCh38
NC_000018.9:g.29102147C>A , CM000680.1:g.29102147C>A	GRCh37
NC_000018.8:g.27356145C>A	NCBI36
NG_007072.3:g.28943C>A , LRG_397:g.28943C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682087.2:n.456C>A
ENST00000682241.2:c.625C>A	ENSP00000507600.2:p.Pro209Thr
ENST00000683614.2:n.456C>A
ENST00000682087.1:c.456C>A
ENST00000682241.1:c.456C>A
ENST00000683614.1:c.456C>A
ENST00000683654.1:c.625C>A	ENSP00000506971.1:p.Pro209Thr
ENST00000684461.1:n.1295C>A
ENST00000261590.13:c.625C>A MANE Select	ENSP00000261590.8:p.Pro209Thr
ENST00000261590.12:c.625C>A	ENSP00000261590.8:p.Pro209Thr
ENST00000585206.1:c.625C>A	ENSP00000462503.1:p.Pro209Thr
NM_001943.3:c.625C>A , LRG_397t1:c.625C>A	NP_001934.2:p.Pro209Thr
NM_001943.4:c.625C>A	NP_001934.2:p.Pro209Thr
XM_024451095.1:c.91C>A	XP_024306863.1:p.Pro31Thr
NM_001943.5:c.625C>A MANE Select	NP_001934.2:p.Pro209Thr