Canonical Allele Identifier: CA2641412728

Gene: DSG2

Linked Data

• gnomAD v4: 18-31521031-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31521037dup , CM000680.2:g.31521037dup	GRCh38
NC_000018.9:g.29101000dup , CM000680.1:g.29101000dup	GRCh37
NC_000018.8:g.27354998dup	NCBI36
NG_007072.3:g.27796dup , LRG_397:g.27796dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000682087.2:n.210-62dup
ENST00000682241.2:c.379-62dup	ENSP00000507600.2:n.379-62dup
ENST00000683614.2:n.210-62dup
ENST00000682087.1:c.210-62dup
ENST00000682241.1:c.210-62dup
ENST00000683614.1:c.210-62dup
ENST00000683654.1:c.379-62dup	ENSP00000506971.1:n.379-62dup
ENST00000684461.1:n.210-62dup
ENST00000261590.13:c.379-62dup MANE Select	ENSP00000261590.8:n.379-62dup
ENST00000261590.12:c.379-62dup	ENSP00000261590.8:n.379-62dup
ENST00000585206.1:c.379-62dup	ENSP00000462503.1:n.379-62dup
NM_001943.3:c.379-62dup , LRG_397t1:c.379-62dup	NP_001934.2:n.379-62dup
NM_001943.4:c.379-62dup	NP_001934.2:n.379-62dup
XM_024451095.1:c.-156-62dup	XP_024306863.1:n.-156-62dup
NM_001943.5:c.379-62dup MANE Select	NP_001934.2:n.379-62dup