Canonical Allele Identifier: CA343454225

Gene: CRP

Linked Data

• MyVariant Identifiers: chr1:g.159683604A>G (hg19) ; chr1:g.159713814A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713814A>G , CM000663.2:g.159713814A>G	GRCh38
NC_000001.10:g.159683604A>G , CM000663.1:g.159683604A>G	GRCh37
NC_000001.9:g.157950228A>G	NCBI36
NG_013007.1:g.5776T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.386T>C MANE Select	ENSP00000255030.5:p.Val129Ala
ENST00000368110.1:c.194-174T>C	ENSP00000357091.1:n.194-174T>C
ENST00000368111.5:c.194-174T>C	ENSP00000357092.1:n.194-174T>C
ENST00000368112.5:c.197+189T>C	ENSP00000357093.1:n.197+189T>C
ENST00000437342.1:c.-149T>C	ENSP00000402788.1:n.-149T>C
ENST00000489317.1:n.74+193T>C
NM_000567.2:c.386T>C	NP_000558.2:p.Val129Ala
XM_011509207.1:c.386T>C	XP_011507509.1:p.Val129Ala
NM_001329057.1:c.386T>C	NP_001315986.1:p.Val129Ala
NM_001329058.1:c.197+189T>C	NP_001315987.1:n.197+189T>C
NM_000567.3:c.386T>C MANE Select	NP_000558.2:p.Val129Ala
NM_001329057.2:c.386T>C	NP_001315986.1:p.Val129Ala
NM_001329058.2:c.197+189T>C	NP_001315987.1:n.197+189T>C
NM_001382703.1:c.194-174T>C	NP_001369632.1:n.194-174T>C