Canonical Allele Identifier: CA1008297620
Gene: CRP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159712344_159712345insCGGTGGTCGCC , CM000663.2:g.159712344_159712345insCGGTGGTCGCC GRCh38
NC_000001.10:g.159682134_159682135insCGGTGGTCGCC , CM000663.1:g.159682134_159682135insCGGTGGTCGCC GRCh37
NC_000001.9:g.157948758_157948759insCGGTGGTCGCC NCBI36
NG_013007.1:g.7245_7246insGGCGACCACCG

Transcript Alleles

HGVS Amino-acid change
ENST00000255030.9:c.*1180_*1181insGGCGACCACCG MANE Select ENSP00000255030.5:n.*1180_*1181insGGCGACC...
ENST00000437342.1:c.*472_*473insGGCGACCACCG ENSP00000402788.1:n.*472_*473insGGCGACCAC...
ENST00000473196.1:n.715_716insGGCGACCACCG
NM_000567.2:c.*1180_*1181insGGCGACCACCG NP_000558.2:n.*1180_*1181insGGCGACCACCG
XM_011509207.1:c.*472_*473insGGCGACCACCG XP_011507509.1:n.*472_*473insGGCGACCACCG
NM_001329057.1:c.*472_*473insGGCGACCACCG NP_001315986.1:n.*472_*473insGGCGACCACCG
NM_001329058.1:c.*246_*247insGGCGACCACCG NP_001315987.1:n.*246_*247insGGCGACCACCG
NM_000567.3:c.*1180_*1181insGGCGACCACCG MANE Select NP_000558.2:n.*1180_*1181insGGCGACCACCG
NM_001329057.2:c.*472_*473insGGCGACCACCG NP_001315986.1:n.*472_*473insGGCGACCACCG
NM_001329058.2:c.*246_*247insGGCGACCACCG NP_001315987.1:n.*246_*247insGGCGACCACCG
NM_001382703.1:c.*1180_*1181insGGCGACCACCG NP_001369632.1:n.*1180_*1181insGGCGACCACC...