Canonical Allele Identifier: CA343453459

Gene: CRP

Linked Data

• MyVariant Identifiers: chr1:g.159683352T>C (hg19) ; chr1:g.159713562T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713562T>C , CM000663.2:g.159713562T>C	GRCh38
NC_000001.10:g.159683352T>C , CM000663.1:g.159683352T>C	GRCh37
NC_000001.9:g.157949976T>C	NCBI36
NG_013007.1:g.6028A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.638A>G MANE Select	ENSP00000255030.5:p.Gln213Arg
ENST00000368110.1:c.272A>G	ENSP00000357091.1:p.Gln91Arg
ENST00000368111.5:c.272A>G	ENSP00000357092.1:p.Gln91Arg
ENST00000368112.5:c.239A>G	ENSP00000357093.1:p.Gln80Arg
ENST00000437342.1:c.104A>G	ENSP00000402788.1:p.Gln35Arg
ENST00000473196.1:n.206A>G
ENST00000489317.1:n.74+445A>G
NM_000567.2:c.638A>G	NP_000558.2:p.Gln213Arg
XM_011509207.1:c.638A>G	XP_011507509.1:p.Gln213Arg
NM_001329057.1:c.638A>G	NP_001315986.1:p.Gln213Arg
NM_001329058.1:c.239A>G	NP_001315987.1:p.Gln80Arg
NM_000567.3:c.638A>G MANE Select	NP_000558.2:p.Gln213Arg
NM_001329057.2:c.638A>G	NP_001315986.1:p.Gln213Arg
NM_001329058.2:c.239A>G	NP_001315987.1:p.Gln80Arg
NM_001382703.1:c.272A>G	NP_001369632.1:p.Gln91Arg