Canonical Allele Identifier: CA656962612
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31547203_31547204insT , CM000680.2:g.31547203_31547204insT GRCh38
NC_000018.9:g.29127166_29127167insT , CM000680.1:g.29127166_29127167insT GRCh37
NC_000018.8:g.27381164_27381165insT NCBI36
NG_007072.3:g.53962_53963insT , LRG_397:g.53962_53963insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.*460_*461insT (DSG2) MANE Select ENSP00000261590.8:n.*460_*461insT
ENST00000261590.12:c.*460_*461insT (DSG2) ENSP00000261590.8:n.*460_*461insT
NM_001943.3:c.*460_*461insT , LRG_397t1:c.*460_*461insT (DSG2) NP_001934.2:n.*460_*461insT
NR_045216.1:n.1346-1298_1346-1297insA (DSG2-AS1)
NM_001943.4:c.*460_*461insT (DSG2) NP_001934.2:n.*460_*461insT
XM_024451095.1:c.*460_*461insT (DSG2) XP_024306863.1:n.*460_*461insT
NM_001943.5:c.*460_*461insT (DSG2) MANE Select NP_001934.2:n.*460_*461insT