Canonical Allele Identifier: CA2648592776
Gene: CRP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159712362_159712363insCCGTGCCAT , CM000663.2:g.159712362_159712363insCCGTGCCAT GRCh38
NC_000001.10:g.159682152_159682153insCCGTGCCAT , CM000663.1:g.159682152_159682153insCCGTGCCAT GRCh37
NC_000001.9:g.157948776_157948777insCCGTGCCAT NCBI36
NG_013007.1:g.7227_7228insATGGCACGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000255030.9:c.*1162_*1163insATGGCACGG MANE Select ENSP00000255030.5:n.*1162_*1163insATGGCACGG
ENST00000437342.1:c.*454_*455insATGGCACGG ENSP00000402788.1:n.*454_*455insATGGCACGG
ENST00000473196.1:n.697_698insATGGCACGG
NM_000567.2:c.*1162_*1163insATGGCACGG NP_000558.2:n.*1162_*1163insATGGCACGG
XM_011509207.1:c.*454_*455insATGGCACGG XP_011507509.1:n.*454_*455insATGGCACGG
NM_001329057.1:c.*454_*455insATGGCACGG NP_001315986.1:n.*454_*455insATGGCACGG
NM_001329058.1:c.*228_*229insATGGCACGG NP_001315987.1:n.*228_*229insATGGCACGG
NM_000567.3:c.*1162_*1163insATGGCACGG MANE Select NP_000558.2:n.*1162_*1163insATGGCACGG
NM_001329057.2:c.*454_*455insATGGCACGG NP_001315986.1:n.*454_*455insATGGCACGG
NM_001329058.2:c.*228_*229insATGGCACGG NP_001315987.1:n.*228_*229insATGGCACGG
NM_001382703.1:c.*1162_*1163insATGGCACGG NP_001369632.1:n.*1162_*1163insATGGCACGG