Canonical Allele Identifier: CA1202014299

Gene: CRP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159712461C= , CM000663.2:g.159712461C=	GRCh38
NC_000001.10:g.159682251C= , CM000663.1:g.159682251C=	GRCh37
NC_000001.9:g.157948875C=	NCBI36
NG_013007.1:g.7129G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000255030.9:c.*1064G= MANE Select	ENSP00000255030.5:n.*1064G=
ENST00000368112.5:c.*356G=	ENSP00000357093.1:n.*356G=
ENST00000437342.1:c.*356G=	ENSP00000402788.1:n.*356G=
ENST00000473196.1:n.599G=
NM_000567.2:c.*1064G=	NP_000558.2:n.*1064G=
XM_011509207.1:c.*356G=	XP_011507509.1:n.*356G=
NM_001329057.1:c.*356G=	NP_001315986.1:n.*356G=
NM_001329058.1:c.*130G=	NP_001315987.1:n.*130G=
NM_000567.3:c.*1064G= MANE Select	NP_000558.2:n.*1064G=
NM_001329057.2:c.*356G=	NP_001315986.1:n.*356G=
NM_001329058.2:c.*130G=	NP_001315987.1:n.*130G=
NM_001382703.1:c.*1064G=	NP_001369632.1:n.*1064G=