Canonical Allele Identifier: CA1202015402

Gene: CRP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713594G= , CM000663.2:g.159713594G=	GRCh38
NC_000001.10:g.159683384G= , CM000663.1:g.159683384G=	GRCh37
NC_000001.9:g.157950008G=	NCBI36
NG_013007.1:g.5996C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.606C= MANE Select	ENSP00000255030.5:p.Val202=
ENST00000368110.1:c.240C=	ENSP00000357091.1:p.Val80=
ENST00000368111.5:c.240C=	ENSP00000357092.1:p.Val80=
ENST00000368112.5:c.207C=	ENSP00000357093.1:p.Val69=
ENST00000437342.1:c.72C=	ENSP00000402788.1:p.Val24=
ENST00000473196.1:n.174C=
ENST00000489317.1:n.74+413C=
NM_000567.2:c.606C=	NP_000558.2:p.Val202=
XM_011509207.1:c.606C=	XP_011507509.1:p.Val202=
NM_001329057.1:c.606C=	NP_001315986.1:p.Val202=
NM_001329058.1:c.207C=	NP_001315987.1:p.Val69=
NM_000567.3:c.606C= MANE Select	NP_000558.2:p.Val202=
NM_001329057.2:c.606C=	NP_001315986.1:p.Val202=
NM_001329058.2:c.207C=	NP_001315987.1:p.Val69=
NM_001382703.1:c.240C=	NP_001369632.1:p.Val80=