Canonical Allele Identifier: CA2746328434

Gene: CRP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159712873G>C , CM000663.2:g.159712873G>C	GRCh38
NC_000001.10:g.159682663G>C , CM000663.1:g.159682663G>C	GRCh37
NC_000001.9:g.157949287G>C	NCBI36
NG_013007.1:g.6717C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.*652C>G MANE Select	ENSP00000255030.5:n.*652C>G
ENST00000368110.1:c.*23-79C>G	ENSP00000357091.1:n.*23-79C>G
ENST00000368111.5:c.*23-293C>G	ENSP00000357092.1:n.*23-293C>G
ENST00000368112.5:c.*23-79C>G	ENSP00000357093.1:n.*23-79C>G
ENST00000437342.1:c.*23-79C>G	ENSP00000402788.1:n.*23-79C>G
ENST00000473196.1:n.266-79C>G
ENST00000489317.1:n.75-79C>G
NM_000567.2:c.*652C>G	NP_000558.2:n.*652C>G
XM_011509207.1:c.*23-79C>G	XP_011507509.1:n.*23-79C>G
NM_001329057.1:c.*23-79C>G	NP_001315986.1:n.*23-79C>G
NM_001329058.1:c.*23-305C>G	NP_001315987.1:n.*23-305C>G
NM_000567.3:c.*652C>G MANE Select	NP_000558.2:n.*652C>G
NM_001329057.2:c.*23-79C>G	NP_001315986.1:n.*23-79C>G
NM_001329058.2:c.*23-305C>G	NP_001315987.1:n.*23-305C>G
NM_001382703.1:c.*652C>G	NP_001369632.1:n.*652C>G