Canonical Allele Identifier: CA1202015179
Gene: CRP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159713405_159713453delinsCCCAGAGACAGAGACGTGGGAACCATGCAGTGTAAAAAAGCGGGAGGTA , CM000663.2:g.159713405_159713453delinsCCCAGAGACAGAGACGTGGGAACCATGCAGTGTAAAAAAGCGGGAGGTA GRCh38
NC_000001.10:g.159683195_159683243delinsCCCAGAGACAGAGACGTGGGAACCATGCAGTGTAAAAAAGCGGGAGGTA , CM000663.1:g.159683195_159683243delinsCCCAGAGACAGAGACGTGGGAACCATGCAGTGTAAAAAAGCGGGAGGTA GRCh37
NC_000001.9:g.157949819_157949867delinsCCCAGAGACAGAGACGTGGGAACCATGCAGTGTAAAAAAGCGGGAGGTA NCBI36
NG_013007.1:g.6137_6185delinsTACCTCCCGCTTTTTTACACTGCATGGTTCCCACGTCTCTGTCTCTGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000255030.9:c.*72_*120delinsTACCTCCCGCTTTTTTACACTGCATGGTTCCCACGTCTCTGTCTCTGGG MANE Select ENSP00000255030.5:n.*72_*120delinsTACCTCCCGCTTTTTTACACTGCATGG...
ENST00000368110.1:c.*22+50_*22+98delinsTACCTCCCGCTTTTTTACACTGCATGGTTCCCACGTCTCTGTCTCTGGG ENSP00000357091.1:n.*22+50_*22+98delinsTACCTCCCGCTTTTTTACACTG...
ENST00000368111.5:c.*22+50_*22+98delinsTACCTCCCGCTTTTTTACACTGCATGGTTCCCACGTCTCTGTCTCTGGG ENSP00000357092.1:n.*22+50_*22+98delinsTACCTCCCGCTTTTTTACACTG...
ENST00000368112.5:c.*22+50_*22+98delinsTACCTCCCGCTTTTTTACACTGCATGGTTCCCACGTCTCTGTCTCTGGG ENSP00000357093.1:n.*22+50_*22+98delinsTACCTCCCGCTTTTTTACACTG...
ENST00000437342.1:c.*22+50_*22+98delinsTACCTCCCGCTTTTTTACACTGCATGGTTCCCACGTCTCTGTCTCTGGG ENSP00000402788.1:n.*22+50_*22+98delinsTACCTCCCGCTTTTTTACACTG...
ENST00000473196.1:n.265+50_265+98delinsTACCTCCCGCTTTTTTACACTGCATGGTTCCCACGTCTCTGTCTCTGGG
ENST00000489317.1:n.74+554_74+602delinsTACCTCCCGCTTTTTTACACTGCATGGTTCCCACGTCTCTGTCTCTGGG
NM_000567.2:c.*72_*120delinsTACCTCCCGCTTTTTTACACTGCATGGTTCCCACGTCTCTGTCTCTGGG NP_000558.2:n.*72_*120delinsTACCTCCCGCTTTTTTACACTGCATGGTTCCCA...
XM_011509207.1:c.*22+50_*22+98delinsTACCTCCCGCTTTTTTACACTGCATGGTTCCCACGTCTCTGTCTCTGGG XP_011507509.1:n.*22+50_*22+98delinsTACCTCCCGCTTTTTTACACTGCAT...
NM_001329057.1:c.*22+50_*22+98delinsTACCTCCCGCTTTTTTACACTGCATGGTTCCCACGTCTCTGTCTCTGGG NP_001315986.1:n.*22+50_*22+98delinsTACCTCCCGCTTTTTTACACTGCAT...
NM_001329058.1:c.*22+50_*22+98delinsTACCTCCCGCTTTTTTACACTGCATGGTTCCCACGTCTCTGTCTCTGGG NP_001315987.1:n.*22+50_*22+98delinsTACCTCCCGCTTTTTTACACTGCAT...
NM_000567.3:c.*72_*120delinsTACCTCCCGCTTTTTTACACTGCATGGTTCCCACGTCTCTGTCTCTGGG MANE Select NP_000558.2:n.*72_*120delinsTACCTCCCGCTTTTTTACACTGCATGGTTCCCA...
NM_001329057.2:c.*22+50_*22+98delinsTACCTCCCGCTTTTTTACACTGCATGGTTCCCACGTCTCTGTCTCTGGG NP_001315986.1:n.*22+50_*22+98delinsTACCTCCCGCTTTTTTACACTGCAT...
NM_001329058.2:c.*22+50_*22+98delinsTACCTCCCGCTTTTTTACACTGCATGGTTCCCACGTCTCTGTCTCTGGG NP_001315987.1:n.*22+50_*22+98delinsTACCTCCCGCTTTTTTACACTGCAT...
NM_001382703.1:c.*72_*120delinsTACCTCCCGCTTTTTTACACTGCATGGTTCCCACGTCTCTGTCTCTGGG NP_001369632.1:n.*72_*120delinsTACCTCCCGCTTTTTTACACTGCATGGTTC...