Canonical Allele Identifier: CA2483404614
Gene: CR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207454390_207454392delinsCAT , CM000663.2:g.207454390_207454392delinsCAT GRCh38
NC_000001.10:g.207627735_207627737delinsCAT , CM000663.1:g.207627735_207627737delinsCAT GRCh37
NC_000001.9:g.205694358_205694360delinsCAT NCBI36
NG_013006.1:g.5091_5093delinsCAT , LRG_348:g.5091_5093delinsCAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000699620.1:c.-471_-469delinsCAT ENSP00000514480.1:n.-471_-469delinsCAT
ENST00000699640.1:c.-385+1295_-385+1297delinsCAT ENSP00000514493.1:n.-385+1295_-385+1297delinsCAT
ENST00000367057.8:c.-29_-27delinsCAT MANE Select ENSP00000356024.3:n.-29_-27delinsCAT
ENST00000367057.7:c.-29_-27delinsCAT ENSP00000356024.3:n.-29_-27delinsCAT
ENST00000367058.7:c.-29_-27delinsCAT ENSP00000356025.3:n.-29_-27delinsCAT
ENST00000367059.3:c.-29_-27delinsCAT ENSP00000356026.3:n.-29_-27delinsCAT
NM_001006658.2:c.-29_-27delinsCAT , LRG_348t1:c.-29_-27delinsCAT NP_001006659.1:n.-29_-27delinsCAT
NM_001877.4:c.-29_-27delinsCAT NP_001868.2:n.-29_-27delinsCAT
NM_001006658.3:c.-29_-27delinsCAT MANE Select NP_001006659.1:n.-29_-27delinsCAT
NM_001877.5:c.-29_-27delinsCAT NP_001868.2:n.-29_-27delinsCAT