Canonical Allele Identifier: CA343453450

Gene: CRP

Linked Data

• MyVariant Identifiers: chr1:g.159683349C>A (hg19) ; chr1:g.159713559C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713559C>A , CM000663.2:g.159713559C>A	GRCh38
NC_000001.10:g.159683349C>A , CM000663.1:g.159683349C>A	GRCh37
NC_000001.9:g.157949973C>A	NCBI36
NG_013007.1:g.6031G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.641G>T MANE Select	ENSP00000255030.5:p.Gly214Val
ENST00000368110.1:c.275G>T	ENSP00000357091.1:p.Gly92Val
ENST00000368111.5:c.275G>T	ENSP00000357092.1:p.Gly92Val
ENST00000368112.5:c.242G>T	ENSP00000357093.1:p.Gly81Val
ENST00000437342.1:c.107G>T	ENSP00000402788.1:p.Gly36Val
ENST00000473196.1:n.209G>T
ENST00000489317.1:n.74+448G>T
NM_000567.2:c.641G>T	NP_000558.2:p.Gly214Val
XM_011509207.1:c.641G>T	XP_011507509.1:p.Gly214Val
NM_001329057.1:c.641G>T	NP_001315986.1:p.Gly214Val
NM_001329058.1:c.242G>T	NP_001315987.1:p.Gly81Val
NM_000567.3:c.641G>T MANE Select	NP_000558.2:p.Gly214Val
NM_001329057.2:c.641G>T	NP_001315986.1:p.Gly214Val
NM_001329058.2:c.242G>T	NP_001315987.1:p.Gly81Val
NM_001382703.1:c.275G>T	NP_001369632.1:p.Gly92Val