Canonical Allele Identifier: CA1202014211
Gene: CRP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159712350C= , CM000663.2:g.159712350C= GRCh38
NC_000001.10:g.159682140C= , CM000663.1:g.159682140C= GRCh37
NC_000001.9:g.157948764C= NCBI36
NG_013007.1:g.7240G=

Transcript Alleles

HGVS Amino-acid change
ENST00000255030.9:c.*1175G= MANE Select ENSP00000255030.5:n.*1175G=
ENST00000437342.1:c.*467G= ENSP00000402788.1:n.*467G=
ENST00000473196.1:n.710G=
NM_000567.2:c.*1175G= NP_000558.2:n.*1175G=
XM_011509207.1:c.*467G= XP_011507509.1:n.*467G=
NM_001329057.1:c.*467G= NP_001315986.1:n.*467G=
NM_001329058.1:c.*241G= NP_001315987.1:n.*241G=
NM_000567.3:c.*1175G= MANE Select NP_000558.2:n.*1175G=
NM_001329057.2:c.*467G= NP_001315986.1:n.*467G=
NM_001329058.2:c.*241G= NP_001315987.1:n.*241G=
NM_001382703.1:c.*1175G= NP_001369632.1:n.*1175G=