Canonical Allele Identifier: CA10651540
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 326493
dbSNP Id: rs146873880

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546874C>T , CM000680.2:g.31546874C>T GRCh38
NC_000018.9:g.29126837C>T , CM000680.1:g.29126837C>T GRCh37
NC_000018.8:g.27380835C>T NCBI36
NG_007072.3:g.53633C>T , LRG_397:g.53633C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261590.13:c.*131C>T (DSG2) MANE Select ENSP00000261590.8:n.*131C>T
ENST00000261590.12:c.*131C>T (DSG2) ENSP00000261590.8:n.*131C>T
NM_001943.3:c.*131C>T , LRG_397t1:c.*131C>T (DSG2) NP_001934.2:n.*131C>T
NR_045216.1:n.1346-968G>A (DSG2-AS1)
NM_001943.4:c.*131C>T (DSG2) NP_001934.2:n.*131C>T
XM_024451095.1:c.*131C>T (DSG2) XP_024306863.1:n.*131C>T
NM_001943.5:c.*131C>T (DSG2) MANE Select NP_001934.2:n.*131C>T