Canonical Allele Identifier: CA2641405689

Gene: DSG2

Linked Data

• gnomAD v4: 18-31498239-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31498239A>G , CM000680.2:g.31498239A>G	GRCh38
NC_000018.9:g.29078202A>G , CM000680.1:g.29078202A>G	GRCh37
NC_000018.8:g.27332200A>G	NCBI36
NG_007072.3:g.4998A>G , LRG_397:g.4998A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682241.2:c.-13A>G	ENSP00000507600.2:n.-13A>G
ENST00000261590.13:c.-13A>G MANE Select	ENSP00000261590.8:n.-13A>G
ENST00000261590.12:c.-13A>G	ENSP00000261590.8:n.-13A>G
ENST00000585206.1:c.-13A>G	ENSP00000462503.1:n.-13A>G
NM_001943.3:c.-13A>G , LRG_397t1:c.-13A>G	NP_001934.2:n.-13A>G
NM_001943.4:c.-13A>G	NP_001934.2:n.-13A>G
NM_001943.5:c.-13A>G MANE Select	NP_001934.2:n.-13A>G