Canonical Allele Identifier: CA2648592916

Gene: CRP

Linked Data

• gnomAD v4: 1-159712456-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159712456T>C , CM000663.2:g.159712456T>C	GRCh38
NC_000001.10:g.159682246T>C , CM000663.1:g.159682246T>C	GRCh37
NC_000001.9:g.157948870T>C	NCBI36
NG_013007.1:g.7134A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000255030.9:c.*1069A>G MANE Select	ENSP00000255030.5:n.*1069A>G
ENST00000368112.5:c.*361A>G	ENSP00000357093.1:n.*361A>G
ENST00000437342.1:c.*361A>G	ENSP00000402788.1:n.*361A>G
ENST00000473196.1:n.604A>G
NM_000567.2:c.*1069A>G	NP_000558.2:n.*1069A>G
XM_011509207.1:c.*361A>G	XP_011507509.1:n.*361A>G
NM_001329057.1:c.*361A>G	NP_001315986.1:n.*361A>G
NM_001329058.1:c.*135A>G	NP_001315987.1:n.*135A>G
NM_000567.3:c.*1069A>G MANE Select	NP_000558.2:n.*1069A>G
NM_001329057.2:c.*361A>G	NP_001315986.1:n.*361A>G
NM_001329058.2:c.*135A>G	NP_001315987.1:n.*135A>G
NM_001382703.1:c.*1069A>G	NP_001369632.1:n.*1069A>G