Canonical Allele Identifier: CA2550734284
Gene: CR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207454406del , CM000663.2:g.207454406del GRCh38
NC_000001.10:g.207627751del , CM000663.1:g.207627751del GRCh37
NC_000001.9:g.205694374del NCBI36
NG_013006.1:g.5107del , LRG_348:g.5107del

Transcript Alleles

HGVS Amino-acid Change
ENST00000699620.1:c.-455del ENSP00000514480.1:n.-455del
ENST00000699640.1:c.-385+1311del ENSP00000514493.1:n.-385+1311del
ENST00000367057.8:c.-13del MANE Select ENSP00000356024.3:n.-13del
ENST00000367057.7:c.-13del ENSP00000356024.3:n.-13del
ENST00000367058.7:c.-13del ENSP00000356025.3:n.-13del
ENST00000367059.3:c.-13del ENSP00000356026.3:n.-13del
NM_001006658.2:c.-13del , LRG_348t1:c.-13del NP_001006659.1:n.-13del
NM_001877.4:c.-13del NP_001868.2:n.-13del
NM_001006658.3:c.-13del MANE Select NP_001006659.1:n.-13del
NM_001877.5:c.-13del NP_001868.2:n.-13del