Canonical Allele Identifier: CA1202014677

Gene: CRP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159712837A= , CM000663.2:g.159712837A=	GRCh38
NC_000001.10:g.159682627A= , CM000663.1:g.159682627A=	GRCh37
NC_000001.9:g.157949251A=	NCBI36
NG_013007.1:g.6753T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.*688T= MANE Select	ENSP00000255030.5:n.*688T=
ENST00000368110.1:c.*23-43T=	ENSP00000357091.1:n.*23-43T=
ENST00000368111.5:c.*23-257T=	ENSP00000357092.1:n.*23-257T=
ENST00000368112.5:c.*23-43T=	ENSP00000357093.1:n.*23-43T=
ENST00000437342.1:c.*23-43T=	ENSP00000402788.1:n.*23-43T=
ENST00000473196.1:n.266-43T=
ENST00000489317.1:n.75-43T=
NM_000567.2:c.*688T=	NP_000558.2:n.*688T=
XM_011509207.1:c.*23-43T=	XP_011507509.1:n.*23-43T=
NM_001329057.1:c.*23-43T=	NP_001315986.1:n.*23-43T=
NM_001329058.1:c.*23-269T=	NP_001315987.1:n.*23-269T=
NM_000567.3:c.*688T= MANE Select	NP_000558.2:n.*688T=
NM_001329057.2:c.*23-43T=	NP_001315986.1:n.*23-43T=
NM_001329058.2:c.*23-269T=	NP_001315987.1:n.*23-269T=
NM_001382703.1:c.*688T=	NP_001369632.1:n.*688T=