Canonical Allele Identifier: CA2648592731
Gene: CRP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159712346_159712347insGTGG , CM000663.2:g.159712346_159712347insGTGG GRCh38
NC_000001.10:g.159682136_159682137insGTGG , CM000663.1:g.159682136_159682137insGTGG GRCh37
NC_000001.9:g.157948760_157948761insGTGG NCBI36
NG_013007.1:g.7246_7247insCCCA

Transcript Alleles

HGVS Amino-acid change
ENST00000255030.9:c.*1181_*1182insCCCA MANE Select ENSP00000255030.5:n.*1181_*1182insCCCA
ENST00000437342.1:c.*473_*474insCCCA ENSP00000402788.1:n.*473_*474insCCCA
ENST00000473196.1:n.716_717insCCCA
NM_000567.2:c.*1181_*1182insCCCA NP_000558.2:n.*1181_*1182insCCCA
XM_011509207.1:c.*473_*474insCCCA XP_011507509.1:n.*473_*474insCCCA
NM_001329057.1:c.*473_*474insCCCA NP_001315986.1:n.*473_*474insCCCA
NM_001329058.1:c.*247_*248insCCCA NP_001315987.1:n.*247_*248insCCCA
NM_000567.3:c.*1181_*1182insCCCA MANE Select NP_000558.2:n.*1181_*1182insCCCA
NM_001329057.2:c.*473_*474insCCCA NP_001315986.1:n.*473_*474insCCCA
NM_001329058.2:c.*247_*248insCCCA NP_001315987.1:n.*247_*248insCCCA
NM_001382703.1:c.*1181_*1182insCCCA NP_001369632.1:n.*1181_*1182insCCCA