Canonical Allele Identifier: CA1202015481

Gene: CRP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713654A= , CM000663.2:g.159713654A=	GRCh38
NC_000001.10:g.159683444A= , CM000663.1:g.159683444A=	GRCh37
NC_000001.9:g.157950068A=	NCBI36
NG_013007.1:g.5936T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.546T= MANE Select	ENSP00000255030.5:p.Phe182=
ENST00000368110.1:c.194-14T=	ENSP00000357091.1:n.194-14T=
ENST00000368111.5:c.194-14T=	ENSP00000357092.1:n.194-14T=
ENST00000368112.5:c.198-51T=	ENSP00000357093.1:n.198-51T=
ENST00000437342.1:c.12T=	ENSP00000402788.1:p.Phe4=
ENST00000473196.1:n.114T=
ENST00000489317.1:n.74+353T=
NM_000567.2:c.546T=	NP_000558.2:p.Phe182=
XM_011509207.1:c.546T=	XP_011507509.1:p.Phe182=
NM_001329057.1:c.546T=	NP_001315986.1:p.Phe182=
NM_001329058.1:c.198-51T=	NP_001315987.1:n.198-51T=
NM_000567.3:c.546T= MANE Select	NP_000558.2:p.Phe182=
NM_001329057.2:c.546T=	NP_001315986.1:p.Phe182=
NM_001329058.2:c.198-51T=	NP_001315987.1:n.198-51T=
NM_001382703.1:c.194-14T=	NP_001369632.1:n.194-14T=