Canonical Allele Identifier: CA2641405672

Gene: DSG2

Linked Data

• gnomAD v4: 18-31498231-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31498231G>T , CM000680.2:g.31498231G>T	GRCh38
NC_000018.9:g.29078194G>T , CM000680.1:g.29078194G>T	GRCh37
NC_000018.8:g.27332192G>T	NCBI36
NG_007072.3:g.4990G>T , LRG_397:g.4990G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682241.2:c.-21G>T	ENSP00000507600.2:n.-21G>T
ENST00000261590.13:c.-21G>T MANE Select	ENSP00000261590.8:n.-21G>T
ENST00000261590.12:c.-21G>T	ENSP00000261590.8:n.-21G>T
ENST00000585206.1:c.-21G>T	ENSP00000462503.1:n.-21G>T
NM_001943.3:c.-21G>T , LRG_397t1:c.-21G>T	NP_001934.2:n.-21G>T
NM_001943.4:c.-21G>T	NP_001934.2:n.-21G>T
NM_001943.5:c.-21G>T MANE Select	NP_001934.2:n.-21G>T