Canonical Allele Identifier: CA2650261389

Gene: CR2

Linked Data

• gnomAD v4: 1-207454381-CTCGGAACGCAT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207454382_207454392del , CM000663.2:g.207454382_207454392del	GRCh38
NC_000001.10:g.207627727_207627737del , CM000663.1:g.207627727_207627737del	GRCh37
NC_000001.9:g.205694350_205694360del	NCBI36
NG_013006.1:g.5083_5093del , LRG_348:g.5083_5093del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699620.1:c.-479_-469del	ENSP00000514480.1:n.-479_-469del
ENST00000699640.1:c.-385+1287_-385+1297del	ENSP00000514493.1:n.-385+1287_-385+1297del
ENST00000367057.8:c.-37_-27del MANE Select	ENSP00000356024.3:n.-37_-27del
ENST00000367057.7:c.-37_-27del	ENSP00000356024.3:n.-37_-27del
ENST00000367058.7:c.-37_-27del	ENSP00000356025.3:n.-37_-27del
ENST00000367059.3:c.-37_-27del	ENSP00000356026.3:n.-37_-27del
NM_001006658.2:c.-37_-27del , LRG_348t1:c.-37_-27del	NP_001006659.1:n.-37_-27del
NM_001877.4:c.-37_-27del	NP_001868.2:n.-37_-27del
NM_001006658.3:c.-37_-27del MANE Select	NP_001006659.1:n.-37_-27del
NM_001877.5:c.-37_-27del	NP_001868.2:n.-37_-27del