Canonical Allele Identifier: CA1008297699
Gene: CRP HGNC NCBI

Linked Data

gnomAD v3: 1-159712354-CAAG-C
gnomAD v4: 1-159712354-CAAG-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159712355_159712357del , CM000663.2:g.159712355_159712357del GRCh38
NC_000001.10:g.159682145_159682147del , CM000663.1:g.159682145_159682147del GRCh37
NC_000001.9:g.157948769_157948771del NCBI36
NG_013007.1:g.7233_7235del

Transcript Alleles

HGVS Amino-acid change
ENST00000255030.9:c.*1168_*1170del MANE Select ENSP00000255030.5:n.*1168_*1170del
ENST00000437342.1:c.*460_*462del ENSP00000402788.1:n.*460_*462del
ENST00000473196.1:n.703_705del
NM_000567.2:c.*1168_*1170del NP_000558.2:n.*1168_*1170del
XM_011509207.1:c.*460_*462del XP_011507509.1:n.*460_*462del
NM_001329057.1:c.*460_*462del NP_001315986.1:n.*460_*462del
NM_001329058.1:c.*234_*236del NP_001315987.1:n.*234_*236del
NM_000567.3:c.*1168_*1170del MANE Select NP_000558.2:n.*1168_*1170del
NM_001329057.2:c.*460_*462del NP_001315986.1:n.*460_*462del
NM_001329058.2:c.*234_*236del NP_001315987.1:n.*234_*236del
NM_001382703.1:c.*1168_*1170del NP_001369632.1:n.*1168_*1170del
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