Canonical Allele Identifier: CA343454413

Gene: CRP

Linked Data

• MyVariant Identifiers: chr1:g.159683686A>C (hg19) ; chr1:g.159713896A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713896A>C , CM000663.2:g.159713896A>C	GRCh38
NC_000001.10:g.159683686A>C , CM000663.1:g.159683686A>C	GRCh37
NC_000001.9:g.157950310A>C	NCBI36
NG_013007.1:g.5694T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.304T>G MANE Select	ENSP00000255030.5:p.Phe102Val
ENST00000368110.1:c.193+111T>G	ENSP00000357091.1:n.193+111T>G
ENST00000368111.5:c.193+111T>G	ENSP00000357092.1:n.193+111T>G
ENST00000368112.5:c.197+107T>G	ENSP00000357093.1:n.197+107T>G
ENST00000437342.1:c.-231T>G	ENSP00000402788.1:n.-231T>G
ENST00000489317.1:n.74+111T>G
NM_000567.2:c.304T>G	NP_000558.2:p.Phe102Val
XM_011509207.1:c.304T>G	XP_011507509.1:p.Phe102Val
NM_001329057.1:c.304T>G	NP_001315986.1:p.Phe102Val
NM_001329058.1:c.197+107T>G	NP_001315987.1:n.197+107T>G
NM_000567.3:c.304T>G MANE Select	NP_000558.2:p.Phe102Val
NM_001329057.2:c.304T>G	NP_001315986.1:p.Phe102Val
NM_001329058.2:c.197+107T>G	NP_001315987.1:n.197+107T>G
NM_001382703.1:c.193+111T>G	NP_001369632.1:n.193+111T>G