Canonical Allele Identifier: CA421617965

Gene: CRP

Linked Data

• gnomAD v4: 1-159713528-G-C
• MyVariant Identifiers: chr1:g.159683318G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713528G>C , CM000663.2:g.159713528G>C	GRCh38
NC_000001.10:g.159683318G>C , CM000663.1:g.159683318G>C	GRCh37
NC_000001.9:g.157949942G>C	NCBI36
NG_013007.1:g.6062C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.672C>G MANE Select	ENSP00000255030.5:p.Pro224=
ENST00000368110.1:c.306C>G	ENSP00000357091.1:p.Pro102=
ENST00000368111.5:c.306C>G	ENSP00000357092.1:p.Pro102=
ENST00000368112.5:c.273C>G	ENSP00000357093.1:p.Pro91=
ENST00000437342.1:c.138C>G	ENSP00000402788.1:p.Pro46=
ENST00000473196.1:n.240C>G
ENST00000489317.1:n.74+479C>G
NM_000567.2:c.672C>G	NP_000558.2:p.Pro224=
XM_011509207.1:c.672C>G	XP_011507509.1:p.Pro224=
NM_001329057.1:c.672C>G	NP_001315986.1:p.Pro224=
NM_001329058.1:c.273C>G	NP_001315987.1:p.Pro91=
NM_000567.3:c.672C>G MANE Select	NP_000558.2:p.Pro224=
NM_001329057.2:c.672C>G	NP_001315986.1:p.Pro224=
NM_001329058.2:c.273C>G	NP_001315987.1:p.Pro91=
NM_001382703.1:c.306C>G	NP_001369632.1:p.Pro102=