Canonical Allele Identifier: CA1008297658
Gene: CRP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159712349_159712356del , CM000663.2:g.159712349_159712356del GRCh38
NC_000001.10:g.159682139_159682146del , CM000663.1:g.159682139_159682146del GRCh37
NC_000001.9:g.157948763_157948770del NCBI36
NG_013007.1:g.7234_7241del

Transcript Alleles

HGVS Amino-acid change
ENST00000255030.9:c.*1169_*1176del MANE Select ENSP00000255030.5:n.*1169_*1176del
ENST00000437342.1:c.*461_*468del ENSP00000402788.1:n.*461_*468del
ENST00000473196.1:n.704_711del
NM_000567.2:c.*1169_*1176del NP_000558.2:n.*1169_*1176del
XM_011509207.1:c.*461_*468del XP_011507509.1:n.*461_*468del
NM_001329057.1:c.*461_*468del NP_001315986.1:n.*461_*468del
NM_001329058.1:c.*235_*242del NP_001315987.1:n.*235_*242del
NM_000567.3:c.*1169_*1176del MANE Select NP_000558.2:n.*1169_*1176del
NM_001329057.2:c.*461_*468del NP_001315986.1:n.*461_*468del
NM_001329058.2:c.*235_*242del NP_001315987.1:n.*235_*242del
NM_001382703.1:c.*1169_*1176del NP_001369632.1:n.*1169_*1176del