Canonical Allele Identifier: CA2648592767

Gene: CRP

Linked Data

• gnomAD v4: 1-159712359-C-CAGGAT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159712359_159712360insAGGAT , CM000663.2:g.159712359_159712360insAGGAT	GRCh38
NC_000001.10:g.159682149_159682150insAGGAT , CM000663.1:g.159682149_159682150insAGGAT	GRCh37
NC_000001.9:g.157948773_157948774insAGGAT	NCBI36
NG_013007.1:g.7230_7231insATCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.*1165_*1166insATCCT MANE Select	ENSP00000255030.5:n.*1165_*1166insATCCT
ENST00000437342.1:c.*457_*458insATCCT	ENSP00000402788.1:n.*457_*458insATCCT
ENST00000473196.1:n.700_701insATCCT
NM_000567.2:c.*1165_*1166insATCCT	NP_000558.2:n.*1165_*1166insATCCT
XM_011509207.1:c.*457_*458insATCCT	XP_011507509.1:n.*457_*458insATCCT
NM_001329057.1:c.*457_*458insATCCT	NP_001315986.1:n.*457_*458insATCCT
NM_001329058.1:c.*231_*232insATCCT	NP_001315987.1:n.*231_*232insATCCT
NM_000567.3:c.*1165_*1166insATCCT MANE Select	NP_000558.2:n.*1165_*1166insATCCT
NM_001329057.2:c.*457_*458insATCCT	NP_001315986.1:n.*457_*458insATCCT
NM_001329058.2:c.*231_*232insATCCT	NP_001315987.1:n.*231_*232insATCCT
NM_001382703.1:c.*1165_*1166insATCCT	NP_001369632.1:n.*1165_*1166insATCCT