Canonical Allele Identifier: CA1008297684
Gene: CRP HGNC NCBI

Linked Data

gnomAD v3: 1-159712352-G-GT
gnomAD v4: 1-159712352-G-GT
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159712352_159712353insT , CM000663.2:g.159712352_159712353insT GRCh38
NC_000001.10:g.159682142_159682143insT , CM000663.1:g.159682142_159682143insT GRCh37
NC_000001.9:g.157948766_157948767insT NCBI36
NG_013007.1:g.7237_7238insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000255030.9:c.*1172_*1173insA MANE Select ENSP00000255030.5:n.*1172_*1173insA
ENST00000437342.1:c.*464_*465insA ENSP00000402788.1:n.*464_*465insA
ENST00000473196.1:n.707_708insA
NM_000567.2:c.*1172_*1173insA NP_000558.2:n.*1172_*1173insA
XM_011509207.1:c.*464_*465insA XP_011507509.1:n.*464_*465insA
NM_001329057.1:c.*464_*465insA NP_001315986.1:n.*464_*465insA
NM_001329058.1:c.*238_*239insA NP_001315987.1:n.*238_*239insA
NM_000567.3:c.*1172_*1173insA MANE Select NP_000558.2:n.*1172_*1173insA
NM_001329057.2:c.*464_*465insA NP_001315986.1:n.*464_*465insA
NM_001329058.2:c.*238_*239insA NP_001315987.1:n.*238_*239insA
NM_001382703.1:c.*1172_*1173insA NP_001369632.1:n.*1172_*1173insA
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