Canonical Allele Identifier: CA421618177

Gene: CRP

Linked Data

• MyVariant Identifiers: chr1:g.159683348G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713558G>T , CM000663.2:g.159713558G>T	GRCh38
NC_000001.10:g.159683348G>T , CM000663.1:g.159683348G>T	GRCh37
NC_000001.9:g.157949972G>T	NCBI36
NG_013007.1:g.6032C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.642C>A MANE Select	ENSP00000255030.5:p.Gly214=
ENST00000368110.1:c.276C>A	ENSP00000357091.1:p.Gly92=
ENST00000368111.5:c.276C>A	ENSP00000357092.1:p.Gly92=
ENST00000368112.5:c.243C>A	ENSP00000357093.1:p.Gly81=
ENST00000437342.1:c.108C>A	ENSP00000402788.1:p.Gly36=
ENST00000473196.1:n.210C>A
ENST00000489317.1:n.74+449C>A
NM_000567.2:c.642C>A	NP_000558.2:p.Gly214=
XM_011509207.1:c.642C>A	XP_011507509.1:p.Gly214=
NM_001329057.1:c.642C>A	NP_001315986.1:p.Gly214=
NM_001329058.1:c.243C>A	NP_001315987.1:p.Gly81=
NM_000567.3:c.642C>A MANE Select	NP_000558.2:p.Gly214=
NM_001329057.2:c.642C>A	NP_001315986.1:p.Gly214=
NM_001329058.2:c.243C>A	NP_001315987.1:p.Gly81=
NM_001382703.1:c.276C>A	NP_001369632.1:p.Gly92=