Canonical Allele Identifier: CA2648593682
Gene: CRP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159713584del , CM000663.2:g.159713584del GRCh38
NC_000001.10:g.159683374del , CM000663.1:g.159683374del GRCh37
NC_000001.9:g.157949998del NCBI36
NG_013007.1:g.6006del

Transcript Alleles

HGVS Amino-acid Change
ENST00000255030.9:c.616del MANE Select ENSP00000255030.5:p.Arg206GlyfsTer3
ENST00000368110.1:c.250del ENSP00000357091.1:p.Arg84GlyfsTer3
ENST00000368111.5:c.250del ENSP00000357092.1:p.Arg84GlyfsTer3
ENST00000368112.5:c.217del ENSP00000357093.1:p.Arg73GlyfsTer3
ENST00000437342.1:c.82del ENSP00000402788.1:p.Arg28GlyfsTer3
ENST00000473196.1:n.184del
ENST00000489317.1:n.74+423del
NM_000567.2:c.616del NP_000558.2:p.Arg206GlyfsTer3
XM_011509207.1:c.616del XP_011507509.1:p.Arg206GlyfsTer3
NM_001329057.1:c.616del NP_001315986.1:p.Arg206GlyfsTer3
NM_001329058.1:c.217del NP_001315987.1:p.Arg73GlyfsTer3
NM_000567.3:c.616del MANE Select NP_000558.2:p.Arg206GlyfsTer3
NM_001329057.2:c.616del NP_001315986.1:p.Arg206GlyfsTer3
NM_001329058.2:c.217del NP_001315987.1:p.Arg73GlyfsTer3
NM_001382703.1:c.250del NP_001369632.1:p.Arg84GlyfsTer3