Canonical Allele Identifier: CA2293866392
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs997183562

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546886T>G , CM000680.2:g.31546886T>G GRCh38
NC_000018.9:g.29126849T>G , CM000680.1:g.29126849T>G GRCh37
NC_000018.8:g.27380847T>G NCBI36
NG_007072.3:g.53645T>G , LRG_397:g.53645T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261590.13:c.*143T>G (DSG2) MANE Select ENSP00000261590.8:n.*143T>G
ENST00000261590.12:c.*143T>G (DSG2) ENSP00000261590.8:n.*143T>G
NM_001943.3:c.*143T>G , LRG_397t1:c.*143T>G (DSG2) NP_001934.2:n.*143T>G
NR_045216.1:n.1346-980A>C (DSG2-AS1)
NM_001943.4:c.*143T>G (DSG2) NP_001934.2:n.*143T>G
XM_024451095.1:c.*143T>G (DSG2) XP_024306863.1:n.*143T>G
NM_001943.5:c.*143T>G (DSG2) MANE Select NP_001934.2:n.*143T>G