Canonical Allele Identifier: CA1146976670

Gene: CRP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713867T= , CM000663.2:g.159713867T=	GRCh38
NC_000001.10:g.159683657T= , CM000663.1:g.159683657T=	GRCh37
NC_000001.9:g.157950281T=	NCBI36
NG_013007.1:g.5723A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.333A= MANE Select	ENSP00000255030.5:p.Pro111=
ENST00000368110.1:c.193+140A=	ENSP00000357091.1:n.193+140A=
ENST00000368111.5:c.193+140A=	ENSP00000357092.1:n.193+140A=
ENST00000368112.5:c.197+136A=	ENSP00000357093.1:n.197+136A=
ENST00000437342.1:c.-202A=	ENSP00000402788.1:n.-202A=
ENST00000489317.1:n.74+140A=
NM_000567.2:c.333A=	NP_000558.2:p.Pro111=
XM_011509207.1:c.333A=	XP_011507509.1:p.Pro111=
NM_001329057.1:c.333A=	NP_001315986.1:p.Pro111=
NM_001329058.1:c.197+136A=	NP_001315987.1:n.197+136A=
NM_000567.3:c.333A= MANE Select	NP_000558.2:p.Pro111=
NM_001329057.2:c.333A=	NP_001315986.1:p.Pro111=
NM_001329058.2:c.197+136A=	NP_001315987.1:n.197+136A=
NM_001382703.1:c.193+140A=	NP_001369632.1:n.193+140A=