Canonical Allele Identifier: CA1202015628

Gene: CRP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713768A= , CM000663.2:g.159713768A=	GRCh38
NC_000001.10:g.159683558A= , CM000663.1:g.159683558A=	GRCh37
NC_000001.9:g.157950182A=	NCBI36
NG_013007.1:g.5822T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.432T= MANE Select	ENSP00000255030.5:p.Thr144=
ENST00000368110.1:c.194-128T=	ENSP00000357091.1:n.194-128T=
ENST00000368111.5:c.194-128T=	ENSP00000357092.1:n.194-128T=
ENST00000368112.5:c.198-165T=	ENSP00000357093.1:n.198-165T=
ENST00000437342.1:c.-103T=	ENSP00000402788.1:n.-103T=
ENST00000489317.1:n.74+239T=
NM_000567.2:c.432T=	NP_000558.2:p.Thr144=
XM_011509207.1:c.432T=	XP_011507509.1:p.Thr144=
NM_001329057.1:c.432T=	NP_001315986.1:p.Thr144=
NM_001329058.1:c.198-165T=	NP_001315987.1:n.198-165T=
NM_000567.3:c.432T= MANE Select	NP_000558.2:p.Thr144=
NM_001329057.2:c.432T=	NP_001315986.1:p.Thr144=
NM_001329058.2:c.198-165T=	NP_001315987.1:n.198-165T=
NM_001382703.1:c.194-128T=	NP_001369632.1:n.194-128T=