Canonical Allele Identifier: CA1202015441

Gene: CRP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713628G= , CM000663.2:g.159713628G=	GRCh38
NC_000001.10:g.159683418G= , CM000663.1:g.159683418G=	GRCh37
NC_000001.9:g.157950042G=	NCBI36
NG_013007.1:g.5962C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.572C= MANE Select	ENSP00000255030.5:p.Thr191=
ENST00000368110.1:c.206C=	ENSP00000357091.1:p.Thr69=
ENST00000368111.5:c.206C=	ENSP00000357092.1:p.Thr69=
ENST00000368112.5:c.198-25C=	ENSP00000357093.1:n.198-25C=
ENST00000437342.1:c.38C=	ENSP00000402788.1:p.Thr13=
ENST00000473196.1:n.140C=
ENST00000489317.1:n.74+379C=
NM_000567.2:c.572C=	NP_000558.2:p.Thr191=
XM_011509207.1:c.572C=	XP_011507509.1:p.Thr191=
NM_001329057.1:c.572C=	NP_001315986.1:p.Thr191=
NM_001329058.1:c.198-25C=	NP_001315987.1:n.198-25C=
NM_000567.3:c.572C= MANE Select	NP_000558.2:p.Thr191=
NM_001329057.2:c.572C=	NP_001315986.1:p.Thr191=
NM_001329058.2:c.198-25C=	NP_001315987.1:n.198-25C=
NM_001382703.1:c.206C=	NP_001369632.1:p.Thr69=