Canonical Allele Identifier: CA344518828

Gene: CR2

Linked Data

• MyVariant Identifiers: chr1:g.207627765T>A (hg19) ; chr1:g.207454420T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207454420T>A , CM000663.2:g.207454420T>A	GRCh38
NC_000001.10:g.207627765T>A , CM000663.1:g.207627765T>A	GRCh37
NC_000001.9:g.205694388T>A	NCBI36
NG_013006.1:g.5121T>A , LRG_348:g.5121T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699620.1:c.-441T>A	ENSP00000514480.1:n.-441T>A
ENST00000699640.1:c.-385+1325T>A	ENSP00000514493.1:n.-385+1325T>A
ENST00000367057.8:c.2T>A MANE Select	ENSP00000356024.3:p.Met1Lys
ENST00000367057.7:c.2T>A	ENSP00000356024.3:p.Met1Lys
ENST00000367058.7:c.2T>A	ENSP00000356025.3:p.Met1Lys
ENST00000367059.3:c.2T>A	ENSP00000356026.3:p.Met1Lys
NM_001006658.2:c.2T>A , LRG_348t1:c.2T>A	NP_001006659.1:p.Met1Lys
NM_001877.4:c.2T>A	NP_001868.2:p.Met1Lys
NM_001006658.3:c.2T>A MANE Select	NP_001006659.1:p.Met1Lys
NM_001877.5:c.2T>A	NP_001868.2:p.Met1Lys