Canonical Allele Identifier: CA2650261410

Gene: CR2

Linked Data

• gnomAD v4: 1-207454400-C-CG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207454405dup , CM000663.2:g.207454405dup	GRCh38
NC_000001.10:g.207627750dup , CM000663.1:g.207627750dup	GRCh37
NC_000001.9:g.205694373dup	NCBI36
NG_013006.1:g.5106dup , LRG_348:g.5106dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699620.1:c.-456dup	ENSP00000514480.1:n.-456dup
ENST00000699640.1:c.-385+1310dup	ENSP00000514493.1:n.-385+1310dup
ENST00000367057.8:c.-14dup MANE Select	ENSP00000356024.3:n.-14dup
ENST00000367057.7:c.-14dup	ENSP00000356024.3:n.-14dup
ENST00000367058.7:c.-14dup	ENSP00000356025.3:n.-14dup
ENST00000367059.3:c.-14dup	ENSP00000356026.3:n.-14dup
NM_001006658.2:c.-14dup , LRG_348t1:c.-14dup	NP_001006659.1:n.-14dup
NM_001877.4:c.-14dup	NP_001868.2:n.-14dup
NM_001006658.3:c.-14dup MANE Select	NP_001006659.1:n.-14dup
NM_001877.5:c.-14dup	NP_001868.2:n.-14dup