Canonical Allele Identifier: CA2648592896

Gene: CRP

Linked Data

• gnomAD v4: 1-159712444-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159712444A>C , CM000663.2:g.159712444A>C	GRCh38
NC_000001.10:g.159682234A>C , CM000663.1:g.159682234A>C	GRCh37
NC_000001.9:g.157948858A>C	NCBI36
NG_013007.1:g.7146T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000255030.9:c.*1081T>G MANE Select	ENSP00000255030.5:n.*1081T>G
ENST00000368112.5:c.*373T>G	ENSP00000357093.1:n.*373T>G
ENST00000437342.1:c.*373T>G	ENSP00000402788.1:n.*373T>G
ENST00000473196.1:n.616T>G
NM_000567.2:c.*1081T>G	NP_000558.2:n.*1081T>G
XM_011509207.1:c.*373T>G	XP_011507509.1:n.*373T>G
NM_001329057.1:c.*373T>G	NP_001315986.1:n.*373T>G
NM_001329058.1:c.*147T>G	NP_001315987.1:n.*147T>G
NM_000567.3:c.*1081T>G MANE Select	NP_000558.2:n.*1081T>G
NM_001329057.2:c.*373T>G	NP_001315986.1:n.*373T>G
NM_001329058.2:c.*147T>G	NP_001315987.1:n.*147T>G
NM_001382703.1:c.*1081T>G	NP_001369632.1:n.*1081T>G