Canonical Allele Identifier: CA1143451365

Gene: CRP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713557C= , CM000663.2:g.159713557C=	GRCh38
NC_000001.10:g.159683347C= , CM000663.1:g.159683347C=	GRCh37
NC_000001.9:g.157949971C=	NCBI36
NG_013007.1:g.6033G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.643G= MANE Select	ENSP00000255030.5:p.Glu215=
ENST00000368110.1:c.277G=	ENSP00000357091.1:p.Glu93=
ENST00000368111.5:c.277G=	ENSP00000357092.1:p.Glu93=
ENST00000368112.5:c.244G=	ENSP00000357093.1:p.Glu82=
ENST00000437342.1:c.109G=	ENSP00000402788.1:p.Glu37=
ENST00000473196.1:n.211G=
ENST00000489317.1:n.74+450G=
NM_000567.2:c.643G=	NP_000558.2:p.Glu215=
XM_011509207.1:c.643G=	XP_011507509.1:p.Glu215=
NM_001329057.1:c.643G=	NP_001315986.1:p.Glu215=
NM_001329058.1:c.244G=	NP_001315987.1:p.Glu82=
NM_000567.3:c.643G= MANE Select	NP_000558.2:p.Glu215=
NM_001329057.2:c.643G=	NP_001315986.1:p.Glu215=
NM_001329058.2:c.244G=	NP_001315987.1:p.Glu82=
NM_001382703.1:c.277G=	NP_001369632.1:p.Glu93=