Canonical Allele Identifier: CA1143647317

Gene: CRP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713894G= , CM000663.2:g.159713894G=	GRCh38
NC_000001.10:g.159683684G= , CM000663.1:g.159683684G=	GRCh37
NC_000001.9:g.157950308G=	NCBI36
NG_013007.1:g.5696C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.306C= MANE Select	ENSP00000255030.5:p.Phe102=
ENST00000368110.1:c.193+113C=	ENSP00000357091.1:n.193+113C=
ENST00000368111.5:c.193+113C=	ENSP00000357092.1:n.193+113C=
ENST00000368112.5:c.197+109C=	ENSP00000357093.1:n.197+109C=
ENST00000437342.1:c.-229C=	ENSP00000402788.1:n.-229C=
ENST00000489317.1:n.74+113C=
NM_000567.2:c.306C=	NP_000558.2:p.Phe102=
XM_011509207.1:c.306C=	XP_011507509.1:p.Phe102=
NM_001329057.1:c.306C=	NP_001315986.1:p.Phe102=
NM_001329058.1:c.197+109C=	NP_001315987.1:n.197+109C=
NM_000567.3:c.306C= MANE Select	NP_000558.2:p.Phe102=
NM_001329057.2:c.306C=	NP_001315986.1:p.Phe102=
NM_001329058.2:c.197+109C=	NP_001315987.1:n.197+109C=
NM_001382703.1:c.193+113C=	NP_001369632.1:n.193+113C=