Canonical Allele Identifier: CA1011643247

Gene: CR2

Linked Data

• dbSNP Id: rs1657773995
• gnomAD v3: 1-207454388-C-CGA
• gnomAD v4: 1-207454388-C-CGA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207454389_207454390insAG , CM000663.2:g.207454389_207454390insAG	GRCh38
NC_000001.10:g.207627734_207627735insAG , CM000663.1:g.207627734_207627735insAG	GRCh37
NC_000001.9:g.205694357_205694358insAG	NCBI36
NG_013006.1:g.5090_5091insAG , LRG_348:g.5090_5091insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699620.1:c.-472_-471insAG	ENSP00000514480.1:n.-472_-471insAG
ENST00000699640.1:c.-385+1294_-385+1295insAG	ENSP00000514493.1:n.-385+1294_-385+1295insAG
ENST00000367057.8:c.-30_-29insAG MANE Select	ENSP00000356024.3:n.-30_-29insAG
ENST00000367057.7:c.-30_-29insAG	ENSP00000356024.3:n.-30_-29insAG
ENST00000367058.7:c.-30_-29insAG	ENSP00000356025.3:n.-30_-29insAG
ENST00000367059.3:c.-30_-29insAG	ENSP00000356026.3:n.-30_-29insAG
NM_001006658.2:c.-30_-29insAG , LRG_348t1:c.-30_-29insAG	NP_001006659.1:n.-30_-29insAG
NM_001877.4:c.-30_-29insAG	NP_001868.2:n.-30_-29insAG
NM_001006658.3:c.-30_-29insAG MANE Select	NP_001006659.1:n.-30_-29insAG
NM_001877.5:c.-30_-29insAG	NP_001868.2:n.-30_-29insAG