Canonical Allele Identifier: CA343454126

Gene: CRP

Linked Data

• MyVariant Identifiers: chr1:g.159683557C>T (hg19) ; chr1:g.159713767C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713767C>T , CM000663.2:g.159713767C>T	GRCh38
NC_000001.10:g.159683557C>T , CM000663.1:g.159683557C>T	GRCh37
NC_000001.9:g.157950181C>T	NCBI36
NG_013007.1:g.5823G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.433G>A MANE Select	ENSP00000255030.5:p.Val145Met
ENST00000368110.1:c.194-127G>A	ENSP00000357091.1:n.194-127G>A
ENST00000368111.5:c.194-127G>A	ENSP00000357092.1:n.194-127G>A
ENST00000368112.5:c.198-164G>A	ENSP00000357093.1:n.198-164G>A
ENST00000437342.1:c.-102G>A	ENSP00000402788.1:n.-102G>A
ENST00000473196.1:n.1G>A
ENST00000489317.1:n.74+240G>A
NM_000567.2:c.433G>A	NP_000558.2:p.Val145Met
XM_011509207.1:c.433G>A	XP_011507509.1:p.Val145Met
NM_001329057.1:c.433G>A	NP_001315986.1:p.Val145Met
NM_001329058.1:c.198-164G>A	NP_001315987.1:n.198-164G>A
NM_000567.3:c.433G>A MANE Select	NP_000558.2:p.Val145Met
NM_001329057.2:c.433G>A	NP_001315986.1:p.Val145Met
NM_001329058.2:c.198-164G>A	NP_001315987.1:n.198-164G>A
NM_001382703.1:c.194-127G>A	NP_001369632.1:n.194-127G>A