Canonical Allele Identifier: CA526652199

Gene: CRP

Linked Data

• dbSNP Id: rs1205433472
• gnomAD v2: 1-159682149-C-CCGTA
• gnomAD v3: 1-159712359-C-CCGTA
• gnomAD v4: 1-159712359-C-CCGTA
• MyVariant Identifiers: chr1:g.159682149_159682150insCGTA (hg19) ; chr1:g.159712359_159712360insCGTA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159712359_159712360insCGTA , CM000663.2:g.159712359_159712360insCGTA	GRCh38
NC_000001.10:g.159682149_159682150insCGTA , CM000663.1:g.159682149_159682150insCGTA	GRCh37
NC_000001.9:g.157948773_157948774insCGTA	NCBI36
NG_013007.1:g.7230_7231insTACG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.*1165_*1166insTACG MANE Select	ENSP00000255030.5:n.*1165_*1166insTACG
ENST00000437342.1:c.*457_*458insTACG	ENSP00000402788.1:n.*457_*458insTACG
ENST00000473196.1:n.700_701insTACG
NM_000567.2:c.*1165_*1166insTACG	NP_000558.2:n.*1165_*1166insTACG
XM_011509207.1:c.*457_*458insTACG	XP_011507509.1:n.*457_*458insTACG
NM_001329057.1:c.*457_*458insTACG	NP_001315986.1:n.*457_*458insTACG
NM_001329058.1:c.*231_*232insTACG	NP_001315987.1:n.*231_*232insTACG
NM_000567.3:c.*1165_*1166insTACG MANE Select	NP_000558.2:n.*1165_*1166insTACG
NM_001329057.2:c.*457_*458insTACG	NP_001315986.1:n.*457_*458insTACG
NM_001329058.2:c.*231_*232insTACG	NP_001315987.1:n.*231_*232insTACG
NM_001382703.1:c.*1165_*1166insTACG	NP_001369632.1:n.*1165_*1166insTACG