Canonical Allele Identifier: CA402127558

Gene: DSG2

Linked Data

• ClinVar Variation Id: 1769342
• ClinVar RCV Id: RCV002380780
• gnomAD v4: 18-31498263-C-G
• MyVariant Identifiers: chr18:g.29078226C>G (hg19) ; chr18:g.31498263C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31498263C>G , CM000680.2:g.31498263C>G	GRCh38
NC_000018.9:g.29078226C>G , CM000680.1:g.29078226C>G	GRCh37
NC_000018.8:g.27332224C>G	NCBI36
NG_007072.3:g.5022C>G , LRG_397:g.5022C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682241.2:c.12C>G	ENSP00000507600.2:p.Ser4Arg
ENST00000683654.1:c.12C>G	ENSP00000506971.1:p.Ser4Arg
ENST00000261590.13:c.12C>G MANE Select	ENSP00000261590.8:p.Ser4Arg
ENST00000261590.12:c.12C>G	ENSP00000261590.8:p.Ser4Arg
ENST00000585206.1:c.12C>G	ENSP00000462503.1:p.Ser4Arg
NM_001943.3:c.12C>G , LRG_397t1:c.12C>G	NP_001934.2:p.Ser4Arg
NM_001943.4:c.12C>G	NP_001934.2:p.Ser4Arg
NM_001943.5:c.12C>G MANE Select	NP_001934.2:p.Ser4Arg