Canonical Allele Identifier: CA2483404558
Gene: CR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207454312_207454314delinsGCC , CM000663.2:g.207454312_207454314delinsGCC GRCh38
NC_000001.10:g.207627657_207627659delinsGCC , CM000663.1:g.207627657_207627659delinsGCC GRCh37
NC_000001.9:g.205694280_205694282delinsGCC NCBI36
NG_013006.1:g.5013_5015delinsGCC , LRG_348:g.5013_5015delinsGCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000699640.1:c.-385+1217_-385+1219delinsGCC ENSP00000514493.1:n.-385+1217_-385+1219delinsGCC
ENST00000367057.7:c.-107_-105delinsGCC ENSP00000356024.3:n.-107_-105delinsGCC
ENST00000367058.7:c.-107_-105delinsGCC ENSP00000356025.3:n.-107_-105delinsGCC
ENST00000367059.3:c.-107_-105delinsGCC ENSP00000356026.3:n.-107_-105delinsGCC
NM_001006658.2:c.-107_-105delinsGCC , LRG_348t1:c.-107_-105delinsGCC NP_001006659.1:n.-107_-105delinsGCC
NM_001877.4:c.-107_-105delinsGCC NP_001868.2:n.-107_-105delinsGCC