Canonical Allele Identifier: CA1202015594

Gene: CRP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713747G= , CM000663.2:g.159713747G=	GRCh38
NC_000001.10:g.159683537G= , CM000663.1:g.159683537G=	GRCh37
NC_000001.9:g.157950161G=	NCBI36
NG_013007.1:g.5843C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.453C= MANE Select	ENSP00000255030.5:p.Ile151=
ENST00000368110.1:c.194-107C=	ENSP00000357091.1:n.194-107C=
ENST00000368111.5:c.194-107C=	ENSP00000357092.1:n.194-107C=
ENST00000368112.5:c.198-144C=	ENSP00000357093.1:n.198-144C=
ENST00000437342.1:c.-82C=	ENSP00000402788.1:n.-82C=
ENST00000473196.1:n.21C=
ENST00000489317.1:n.74+260C=
NM_000567.2:c.453C=	NP_000558.2:p.Ile151=
XM_011509207.1:c.453C=	XP_011507509.1:p.Ile151=
NM_001329057.1:c.453C=	NP_001315986.1:p.Ile151=
NM_001329058.1:c.198-144C=	NP_001315987.1:n.198-144C=
NM_000567.3:c.453C= MANE Select	NP_000558.2:p.Ile151=
NM_001329057.2:c.453C=	NP_001315986.1:p.Ile151=
NM_001329058.2:c.198-144C=	NP_001315987.1:n.198-144C=
NM_001382703.1:c.194-107C=	NP_001369632.1:n.194-107C=