Canonical Allele Identifier: CA2293854943

Gene: DSG2

Linked Data

• dbSNP Id: rs1332379061
• gnomAD v4: 18-31519799-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31519799A>T , CM000680.2:g.31519799A>T	GRCh38
NC_000018.9:g.29099762A>T , CM000680.1:g.29099762A>T	GRCh37
NC_000018.8:g.27353760A>T	NCBI36
NG_007072.3:g.26558A>T , LRG_397:g.26558A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682241.2:c.82-4A>T	ENSP00000507600.2:n.82-4A>T
ENST00000683654.1:c.82-4A>T	ENSP00000506971.1:n.82-4A>T
ENST00000261590.13:c.82-4A>T MANE Select	ENSP00000261590.8:n.82-4A>T
ENST00000261590.12:c.82-4A>T	ENSP00000261590.8:n.82-4A>T
ENST00000585206.1:c.82-4A>T	ENSP00000462503.1:n.82-4A>T
NM_001943.3:c.82-4A>T , LRG_397t1:c.82-4A>T	NP_001934.2:n.82-4A>T
NM_001943.4:c.82-4A>T	NP_001934.2:n.82-4A>T
XM_024451095.1:c.-453-4A>T	XP_024306863.1:n.-453-4A>T
NM_001943.5:c.82-4A>T MANE Select	NP_001934.2:n.82-4A>T