Canonical Allele Identifier: CA1202015702

Gene: CRP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713809C= , CM000663.2:g.159713809C=	GRCh38
NC_000001.10:g.159683599C= , CM000663.1:g.159683599C=	GRCh37
NC_000001.9:g.157950223C=	NCBI36
NG_013007.1:g.5781G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.391G= MANE Select	ENSP00000255030.5:p.Gly131=
ENST00000368110.1:c.194-169G=	ENSP00000357091.1:n.194-169G=
ENST00000368111.5:c.194-169G=	ENSP00000357092.1:n.194-169G=
ENST00000368112.5:c.197+194G=	ENSP00000357093.1:n.197+194G=
ENST00000437342.1:c.-144G=	ENSP00000402788.1:n.-144G=
ENST00000489317.1:n.74+198G=
NM_000567.2:c.391G=	NP_000558.2:p.Gly131=
XM_011509207.1:c.391G=	XP_011507509.1:p.Gly131=
NM_001329057.1:c.391G=	NP_001315986.1:p.Gly131=
NM_001329058.1:c.197+194G=	NP_001315987.1:n.197+194G=
NM_000567.3:c.391G= MANE Select	NP_000558.2:p.Gly131=
NM_001329057.2:c.391G=	NP_001315986.1:p.Gly131=
NM_001329058.2:c.197+194G=	NP_001315987.1:n.197+194G=
NM_001382703.1:c.194-169G=	NP_001369632.1:n.194-169G=