Canonical Allele Identifier: CA402130805

Gene: DSG2

Linked Data

• dbSNP Id: rs397516702
• MyVariant Identifiers: chr18:g.29099836G>A (hg19) ; chr18:g.31519873G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31519873G>A , CM000680.2:g.31519873G>A	GRCh38
NC_000018.9:g.29099836G>A , CM000680.1:g.29099836G>A	GRCh37
NC_000018.8:g.27353834G>A	NCBI36
NG_007072.3:g.26632G>A , LRG_397:g.26632G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682241.2:c.152G>A	ENSP00000507600.2:p.Trp51Ter
ENST00000683654.1:c.152G>A	ENSP00000506971.1:p.Trp51Ter
ENST00000261590.13:c.152G>A MANE Select	ENSP00000261590.8:p.Trp51Ter
ENST00000261590.12:c.152G>A	ENSP00000261590.8:p.Trp51Ter
ENST00000585206.1:c.152G>A	ENSP00000462503.1:p.Trp51Ter
NM_001943.3:c.152G>A , LRG_397t1:c.152G>A	NP_001934.2:p.Trp51Ter
NM_001943.4:c.152G>A	NP_001934.2:p.Trp51Ter
XM_024451095.1:c.-383G>A	XP_024306863.1:n.-383G>A
NM_001943.5:c.152G>A MANE Select	NP_001934.2:p.Trp51Ter