Canonical Allele Identifier: CA1202014217
Gene: CRP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159712355A= , CM000663.2:g.159712355A= GRCh38
NC_000001.10:g.159682145A= , CM000663.1:g.159682145A= GRCh37
NC_000001.9:g.157948769A= NCBI36
NG_013007.1:g.7235T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000255030.9:c.*1170T= MANE Select ENSP00000255030.5:n.*1170T=
ENST00000437342.1:c.*462T= ENSP00000402788.1:n.*462T=
ENST00000473196.1:n.705T=
NM_000567.2:c.*1170T= NP_000558.2:n.*1170T=
XM_011509207.1:c.*462T= XP_011507509.1:n.*462T=
NM_001329057.1:c.*462T= NP_001315986.1:n.*462T=
NM_001329058.1:c.*236T= NP_001315987.1:n.*236T=
NM_000567.3:c.*1170T= MANE Select NP_000558.2:n.*1170T=
NM_001329057.2:c.*462T= NP_001315986.1:n.*462T=
NM_001329058.2:c.*236T= NP_001315987.1:n.*236T=
NM_001382703.1:c.*1170T= NP_001369632.1:n.*1170T=