Canonical Allele Identifier: CA1008297670
Gene: CRP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159712350_159712352del , CM000663.2:g.159712350_159712352del GRCh38
NC_000001.10:g.159682140_159682142del , CM000663.1:g.159682140_159682142del GRCh37
NC_000001.9:g.157948764_157948766del NCBI36
NG_013007.1:g.7238_7240del

Transcript Alleles

HGVS Amino-acid change
ENST00000255030.9:c.*1173_*1175del MANE Select ENSP00000255030.5:n.*1173_*1175del
ENST00000437342.1:c.*465_*467del ENSP00000402788.1:n.*465_*467del
ENST00000473196.1:n.708_710del
NM_000567.2:c.*1173_*1175del NP_000558.2:n.*1173_*1175del
XM_011509207.1:c.*465_*467del XP_011507509.1:n.*465_*467del
NM_001329057.1:c.*465_*467del NP_001315986.1:n.*465_*467del
NM_001329058.1:c.*239_*241del NP_001315987.1:n.*239_*241del
NM_000567.3:c.*1173_*1175del MANE Select NP_000558.2:n.*1173_*1175del
NM_001329057.2:c.*465_*467del NP_001315986.1:n.*465_*467del
NM_001329058.2:c.*239_*241del NP_001315987.1:n.*239_*241del
NM_001382703.1:c.*1173_*1175del NP_001369632.1:n.*1173_*1175del