Canonical Allele Identifier: CA2648592746

Gene: CRP

Linked Data

• gnomAD v4: 1-159712350-C-CGT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159712350_159712351insGT , CM000663.2:g.159712350_159712351insGT	GRCh38
NC_000001.10:g.159682140_159682141insGT , CM000663.1:g.159682140_159682141insGT	GRCh37
NC_000001.9:g.157948764_157948765insGT	NCBI36
NG_013007.1:g.7239_7240insAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000255030.9:c.*1174_*1175insAC MANE Select	ENSP00000255030.5:n.*1174_*1175insAC
ENST00000437342.1:c.*466_*467insAC	ENSP00000402788.1:n.*466_*467insAC
ENST00000473196.1:n.709_710insAC
NM_000567.2:c.*1174_*1175insAC	NP_000558.2:n.*1174_*1175insAC
XM_011509207.1:c.*466_*467insAC	XP_011507509.1:n.*466_*467insAC
NM_001329057.1:c.*466_*467insAC	NP_001315986.1:n.*466_*467insAC
NM_001329058.1:c.*240_*241insAC	NP_001315987.1:n.*240_*241insAC
NM_000567.3:c.*1174_*1175insAC MANE Select	NP_000558.2:n.*1174_*1175insAC
NM_001329057.2:c.*466_*467insAC	NP_001315986.1:n.*466_*467insAC
NM_001329058.2:c.*240_*241insAC	NP_001315987.1:n.*240_*241insAC
NM_001382703.1:c.*1174_*1175insAC	NP_001369632.1:n.*1174_*1175insAC