Canonical Allele Identifier: CA1008297657
Gene: CRP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159712349_159712350insGC , CM000663.2:g.159712349_159712350insGC GRCh38
NC_000001.10:g.159682139_159682140insGC , CM000663.1:g.159682139_159682140insGC GRCh37
NC_000001.9:g.157948763_157948764insGC NCBI36
NG_013007.1:g.7241_7242insCG

Transcript Alleles

HGVS Amino-acid change
ENST00000255030.9:c.*1176_*1177insCG MANE Select ENSP00000255030.5:n.*1176_*1177insCG
ENST00000437342.1:c.*468_*469insCG ENSP00000402788.1:n.*468_*469insCG
ENST00000473196.1:n.711_712insCG
NM_000567.2:c.*1176_*1177insCG NP_000558.2:n.*1176_*1177insCG
XM_011509207.1:c.*468_*469insCG XP_011507509.1:n.*468_*469insCG
NM_001329057.1:c.*468_*469insCG NP_001315986.1:n.*468_*469insCG
NM_001329058.1:c.*242_*243insCG NP_001315987.1:n.*242_*243insCG
NM_000567.3:c.*1176_*1177insCG MANE Select NP_000558.2:n.*1176_*1177insCG
NM_001329057.2:c.*468_*469insCG NP_001315986.1:n.*468_*469insCG
NM_001329058.2:c.*242_*243insCG NP_001315987.1:n.*242_*243insCG
NM_001382703.1:c.*1176_*1177insCG NP_001369632.1:n.*1176_*1177insCG