Canonical Allele Identifier: CA1202015122

Gene: CRP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713347C= , CM000663.2:g.159713347C=	GRCh38
NC_000001.10:g.159683137C= , CM000663.1:g.159683137C=	GRCh37
NC_000001.9:g.157949761C=	NCBI36
NG_013007.1:g.6243G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.*178G= MANE Select	ENSP00000255030.5:n.*178G=
ENST00000368110.1:c.*22+156G=	ENSP00000357091.1:n.*22+156G=
ENST00000368111.5:c.*22+156G=	ENSP00000357092.1:n.*22+156G=
ENST00000368112.5:c.*22+156G=	ENSP00000357093.1:n.*22+156G=
ENST00000437342.1:c.*22+156G=	ENSP00000402788.1:n.*22+156G=
ENST00000473196.1:n.265+156G=
ENST00000489317.1:n.75-553G=
NM_000567.2:c.*178G=	NP_000558.2:n.*178G=
XM_011509207.1:c.*22+156G=	XP_011507509.1:n.*22+156G=
NM_001329057.1:c.*22+156G=	NP_001315986.1:n.*22+156G=
NM_001329058.1:c.*22+156G=	NP_001315987.1:n.*22+156G=
NM_000567.3:c.*178G= MANE Select	NP_000558.2:n.*178G=
NM_001329057.2:c.*22+156G=	NP_001315986.1:n.*22+156G=
NM_001329058.2:c.*22+156G=	NP_001315987.1:n.*22+156G=
NM_001382703.1:c.*178G=	NP_001369632.1:n.*178G=