Canonical Allele Identifier: CA2648592737
Gene: CRP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159712347_159712348insGC , CM000663.2:g.159712347_159712348insGC GRCh38
NC_000001.10:g.159682137_159682138insGC , CM000663.1:g.159682137_159682138insGC GRCh37
NC_000001.9:g.157948761_157948762insGC NCBI36
NG_013007.1:g.7242_7243insGC

Transcript Alleles

HGVS Amino-acid change
ENST00000255030.9:c.*1177_*1178insGC MANE Select ENSP00000255030.5:n.*1177_*1178insGC
ENST00000437342.1:c.*469_*470insGC ENSP00000402788.1:n.*469_*470insGC
ENST00000473196.1:n.712_713insGC
NM_000567.2:c.*1177_*1178insGC NP_000558.2:n.*1177_*1178insGC
XM_011509207.1:c.*469_*470insGC XP_011507509.1:n.*469_*470insGC
NM_001329057.1:c.*469_*470insGC NP_001315986.1:n.*469_*470insGC
NM_001329058.1:c.*243_*244insGC NP_001315987.1:n.*243_*244insGC
NM_000567.3:c.*1177_*1178insGC MANE Select NP_000558.2:n.*1177_*1178insGC
NM_001329057.2:c.*469_*470insGC NP_001315986.1:n.*469_*470insGC
NM_001329058.2:c.*243_*244insGC NP_001315987.1:n.*243_*244insGC
NM_001382703.1:c.*1177_*1178insGC NP_001369632.1:n.*1177_*1178insGC