Canonical Allele Identifier: CA2648593182

Gene: CRP

Linked Data

• gnomAD v4: 1-159712970-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159712970_159712971insC , CM000663.2:g.159712970_159712971insC	GRCh38
NC_000001.10:g.159682760_159682761insC , CM000663.1:g.159682760_159682761insC	GRCh37
NC_000001.9:g.157949384_157949385insC	NCBI36
NG_013007.1:g.6619_6620insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.*554_*555insG MANE Select	ENSP00000255030.5:n.*554_*555insG
ENST00000368110.1:c.*23-177_*23-176insG	ENSP00000357091.1:n.*23-177_*23-176insG
ENST00000368111.5:c.*23-391_*23-390insG	ENSP00000357092.1:n.*23-391_*23-390insG
ENST00000368112.5:c.*23-177_*23-176insG	ENSP00000357093.1:n.*23-177_*23-176insG
ENST00000437342.1:c.*23-177_*23-176insG	ENSP00000402788.1:n.*23-177_*23-176insG
ENST00000473196.1:n.266-177_266-176insG
ENST00000489317.1:n.75-177_75-176insG
NM_000567.2:c.*554_*555insG	NP_000558.2:n.*554_*555insG
XM_011509207.1:c.*23-177_*23-176insG	XP_011507509.1:n.*23-177_*23-176insG
NM_001329057.1:c.*23-177_*23-176insG	NP_001315986.1:n.*23-177_*23-176insG
NM_001329058.1:c.*23-403_*23-402insG	NP_001315987.1:n.*23-403_*23-402insG
NM_000567.3:c.*554_*555insG MANE Select	NP_000558.2:n.*554_*555insG
NM_001329057.2:c.*23-177_*23-176insG	NP_001315986.1:n.*23-177_*23-176insG
NM_001329058.2:c.*23-403_*23-402insG	NP_001315987.1:n.*23-403_*23-402insG
NM_001382703.1:c.*554_*555insG	NP_001369632.1:n.*554_*555insG