Canonical Allele Identifier: CA2648592769

Gene: CRP

Linked Data

• gnomAD v4: 1-159712360-T-TATC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159712360_159712361insATC , CM000663.2:g.159712360_159712361insATC	GRCh38
NC_000001.10:g.159682150_159682151insATC , CM000663.1:g.159682150_159682151insATC	GRCh37
NC_000001.9:g.157948774_157948775insATC	NCBI36
NG_013007.1:g.7229_7230insGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.*1164_*1165insGAT MANE Select	ENSP00000255030.5:n.*1164_*1165insGAT
ENST00000437342.1:c.*456_*457insGAT	ENSP00000402788.1:n.*456_*457insGAT
ENST00000473196.1:n.699_700insGAT
NM_000567.2:c.*1164_*1165insGAT	NP_000558.2:n.*1164_*1165insGAT
XM_011509207.1:c.*456_*457insGAT	XP_011507509.1:n.*456_*457insGAT
NM_001329057.1:c.*456_*457insGAT	NP_001315986.1:n.*456_*457insGAT
NM_001329058.1:c.*230_*231insGAT	NP_001315987.1:n.*230_*231insGAT
NM_000567.3:c.*1164_*1165insGAT MANE Select	NP_000558.2:n.*1164_*1165insGAT
NM_001329057.2:c.*456_*457insGAT	NP_001315986.1:n.*456_*457insGAT
NM_001329058.2:c.*230_*231insGAT	NP_001315987.1:n.*230_*231insGAT
NM_001382703.1:c.*1164_*1165insGAT	NP_001369632.1:n.*1164_*1165insGAT