Canonical Allele Identifier: CA042568
Gene: DSG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 258494
dbSNP Id: rs778100657

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31536257C>T , CM000680.2:g.31536257C>T GRCh38
NC_000018.9:g.29116220C>T , CM000680.1:g.29116220C>T GRCh37
NC_000018.8:g.27370218C>T NCBI36
NG_007072.3:g.43016C>T , LRG_397:g.43016C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.1479C>T MANE Select ENSP00000261590.8:p.Asn493=
ENST00000261590.12:c.1479C>T ENSP00000261590.8:p.Asn493=
NM_001943.3:c.1479C>T , LRG_397t1:c.1479C>T NP_001934.2:p.Asn493=
NM_001943.4:c.1479C>T NP_001934.2:p.Asn493=
XM_024451095.1:c.945C>T XP_024306863.1:p.Asn315=
NM_001943.5:c.1479C>T MANE Select NP_001934.2:p.Asn493=