Canonical Allele Identifier: CA343453433

Gene: CRP

Linked Data

• MyVariant Identifiers: chr1:g.159683340A>G (hg19) ; chr1:g.159713550A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713550A>G , CM000663.2:g.159713550A>G	GRCh38
NC_000001.10:g.159683340A>G , CM000663.1:g.159683340A>G	GRCh37
NC_000001.9:g.157949964A>G	NCBI36
NG_013007.1:g.6040T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.650T>C MANE Select	ENSP00000255030.5:p.Phe217Ser
ENST00000368110.1:c.284T>C	ENSP00000357091.1:p.Phe95Ser
ENST00000368111.5:c.284T>C	ENSP00000357092.1:p.Phe95Ser
ENST00000368112.5:c.251T>C	ENSP00000357093.1:p.Phe84Ser
ENST00000437342.1:c.116T>C	ENSP00000402788.1:p.Phe39Ser
ENST00000473196.1:n.218T>C
ENST00000489317.1:n.74+457T>C
NM_000567.2:c.650T>C	NP_000558.2:p.Phe217Ser
XM_011509207.1:c.650T>C	XP_011507509.1:p.Phe217Ser
NM_001329057.1:c.650T>C	NP_001315986.1:p.Phe217Ser
NM_001329058.1:c.251T>C	NP_001315987.1:p.Phe84Ser
NM_000567.3:c.650T>C MANE Select	NP_000558.2:p.Phe217Ser
NM_001329057.2:c.650T>C	NP_001315986.1:p.Phe217Ser
NM_001329058.2:c.251T>C	NP_001315987.1:p.Phe84Ser
NM_001382703.1:c.284T>C	NP_001369632.1:p.Phe95Ser