Canonical Allele Identifier: CA1202015799

Gene: CRP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713853G= , CM000663.2:g.159713853G=	GRCh38
NC_000001.10:g.159683643G= , CM000663.1:g.159683643G=	GRCh37
NC_000001.9:g.157950267G=	NCBI36
NG_013007.1:g.5737C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.347C= MANE Select	ENSP00000255030.5:p.Thr116=
ENST00000368110.1:c.193+154C=	ENSP00000357091.1:n.193+154C=
ENST00000368111.5:c.193+154C=	ENSP00000357092.1:n.193+154C=
ENST00000368112.5:c.197+150C=	ENSP00000357093.1:n.197+150C=
ENST00000437342.1:c.-188C=	ENSP00000402788.1:n.-188C=
ENST00000489317.1:n.74+154C=
NM_000567.2:c.347C=	NP_000558.2:p.Thr116=
XM_011509207.1:c.347C=	XP_011507509.1:p.Thr116=
NM_001329057.1:c.347C=	NP_001315986.1:p.Thr116=
NM_001329058.1:c.197+150C=	NP_001315987.1:n.197+150C=
NM_000567.3:c.347C= MANE Select	NP_000558.2:p.Thr116=
NM_001329057.2:c.347C=	NP_001315986.1:p.Thr116=
NM_001329058.2:c.197+150C=	NP_001315987.1:n.197+150C=
NM_001382703.1:c.193+154C=	NP_001369632.1:n.193+154C=