Canonical Allele Identifier: CA1202014303

Gene: CRP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159712464A= , CM000663.2:g.159712464A=	GRCh38
NC_000001.10:g.159682254A= , CM000663.1:g.159682254A=	GRCh37
NC_000001.9:g.157948878A=	NCBI36
NG_013007.1:g.7126T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000255030.9:c.*1061T= MANE Select	ENSP00000255030.5:n.*1061T=
ENST00000368112.5:c.*353T=	ENSP00000357093.1:n.*353T=
ENST00000437342.1:c.*353T=	ENSP00000402788.1:n.*353T=
ENST00000473196.1:n.596T=
NM_000567.2:c.*1061T=	NP_000558.2:n.*1061T=
XM_011509207.1:c.*353T=	XP_011507509.1:n.*353T=
NM_001329057.1:c.*353T=	NP_001315986.1:n.*353T=
NM_001329058.1:c.*127T=	NP_001315987.1:n.*127T=
NM_000567.3:c.*1061T= MANE Select	NP_000558.2:n.*1061T=
NM_001329057.2:c.*353T=	NP_001315986.1:n.*353T=
NM_001329058.2:c.*127T=	NP_001315987.1:n.*127T=
NM_001382703.1:c.*1061T=	NP_001369632.1:n.*1061T=