Canonical Allele Identifier: CA343453529

Gene: CRP

Linked Data

• MyVariant Identifiers: chr1:g.159683385A>G (hg19) ; chr1:g.159713595A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713595A>G , CM000663.2:g.159713595A>G	GRCh38
NC_000001.10:g.159683385A>G , CM000663.1:g.159683385A>G	GRCh37
NC_000001.9:g.157950009A>G	NCBI36
NG_013007.1:g.5995T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.605T>C MANE Select	ENSP00000255030.5:p.Val202Ala
ENST00000368110.1:c.239T>C	ENSP00000357091.1:p.Val80Ala
ENST00000368111.5:c.239T>C	ENSP00000357092.1:p.Val80Ala
ENST00000368112.5:c.206T>C	ENSP00000357093.1:p.Val69Ala
ENST00000437342.1:c.71T>C	ENSP00000402788.1:p.Val24Ala
ENST00000473196.1:n.173T>C
ENST00000489317.1:n.74+412T>C
NM_000567.2:c.605T>C	NP_000558.2:p.Val202Ala
XM_011509207.1:c.605T>C	XP_011507509.1:p.Val202Ala
NM_001329057.1:c.605T>C	NP_001315986.1:p.Val202Ala
NM_001329058.1:c.206T>C	NP_001315987.1:p.Val69Ala
NM_000567.3:c.605T>C MANE Select	NP_000558.2:p.Val202Ala
NM_001329057.2:c.605T>C	NP_001315986.1:p.Val202Ala
NM_001329058.2:c.206T>C	NP_001315987.1:p.Val69Ala
NM_001382703.1:c.239T>C	NP_001369632.1:p.Val80Ala