Canonical Allele Identifier: CA778425917
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1282632229

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546888C>T , CM000680.2:g.31546888C>T GRCh38
NC_000018.9:g.29126851C>T , CM000680.1:g.29126851C>T GRCh37
NC_000018.8:g.27380849C>T NCBI36
NG_007072.3:g.53647C>T , LRG_397:g.53647C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261590.13:c.*145C>T (DSG2) MANE Select ENSP00000261590.8:n.*145C>T
ENST00000261590.12:c.*145C>T (DSG2) ENSP00000261590.8:n.*145C>T
NM_001943.3:c.*145C>T , LRG_397t1:c.*145C>T (DSG2) NP_001934.2:n.*145C>T
NR_045216.1:n.1346-982G>A (DSG2-AS1)
NM_001943.4:c.*145C>T (DSG2) NP_001934.2:n.*145C>T
XM_024451095.1:c.*145C>T (DSG2) XP_024306863.1:n.*145C>T
NM_001943.5:c.*145C>T (DSG2) MANE Select NP_001934.2:n.*145C>T