Canonical Allele Identifier: CA2565866667

Gene: CR2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207454410_207454411insA , CM000663.2:g.207454410_207454411insA	GRCh38
NC_000001.10:g.207627755_207627756insA , CM000663.1:g.207627755_207627756insA	GRCh37
NC_000001.9:g.205694378_205694379insA	NCBI36
NG_013006.1:g.5111_5112insA , LRG_348:g.5111_5112insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699620.1:c.-451_-450insA	ENSP00000514480.1:n.-451_-450insA
ENST00000699640.1:c.-385+1315_-385+1316insA	ENSP00000514493.1:n.-385+1315_-385+1316insA
ENST00000367057.8:c.-9_-8insA MANE Select	ENSP00000356024.3:n.-9_-8insA
ENST00000367057.7:c.-9_-8insA	ENSP00000356024.3:n.-9_-8insA
ENST00000367058.7:c.-9_-8insA	ENSP00000356025.3:n.-9_-8insA
ENST00000367059.3:c.-9_-8insA	ENSP00000356026.3:n.-9_-8insA
NM_001006658.2:c.-9_-8insA , LRG_348t1:c.-9_-8insA	NP_001006659.1:n.-9_-8insA
NM_001877.4:c.-9_-8insA	NP_001868.2:n.-9_-8insA
NM_001006658.3:c.-9_-8insA MANE Select	NP_001006659.1:n.-9_-8insA
NM_001877.5:c.-9_-8insA	NP_001868.2:n.-9_-8insA