Canonical Allele Identifier: CA2648593188

Gene: CRP

Linked Data

• gnomAD v4: 1-159712972-T-TACCCAGAACTCCA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159712972_159712973insACCCAGAACTCCA , CM000663.2:g.159712972_159712973insACCCAGAACTCCA	GRCh38
NC_000001.10:g.159682762_159682763insACCCAGAACTCCA , CM000663.1:g.159682762_159682763insACCCAGAACTCCA	GRCh37
NC_000001.9:g.157949386_157949387insACCCAGAACTCCA	NCBI36
NG_013007.1:g.6617_6618insTGGAGTTCTGGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.*552_*553insTGGAGTTCTGGGT MANE Select	ENSP00000255030.5:n.*552_*553insTGGAGTTCTGGGT
ENST00000368110.1:c.*23-179_*23-178insTGGAGTTCTGGGT	ENSP00000357091.1:n.*23-179_*23-178insTGGAGTTCTGGGT
ENST00000368111.5:c.*23-393_*23-392insTGGAGTTCTGGGT	ENSP00000357092.1:n.*23-393_*23-392insTGGAGTTCTGGGT
ENST00000368112.5:c.*23-179_*23-178insTGGAGTTCTGGGT	ENSP00000357093.1:n.*23-179_*23-178insTGGAGTTCTGGGT
ENST00000437342.1:c.*23-179_*23-178insTGGAGTTCTGGGT	ENSP00000402788.1:n.*23-179_*23-178insTGGAGTTCTGGGT
ENST00000473196.1:n.266-179_266-178insTGGAGTTCTGGGT
ENST00000489317.1:n.75-179_75-178insTGGAGTTCTGGGT
NM_000567.2:c.*552_*553insTGGAGTTCTGGGT	NP_000558.2:n.*552_*553insTGGAGTTCTGGGT
XM_011509207.1:c.*23-179_*23-178insTGGAGTTCTGGGT	XP_011507509.1:n.*23-179_*23-178insTGGAGTTCTGGGT
NM_001329057.1:c.*23-179_*23-178insTGGAGTTCTGGGT	NP_001315986.1:n.*23-179_*23-178insTGGAGTTCTGGGT
NM_001329058.1:c.*23-405_*23-404insTGGAGTTCTGGGT	NP_001315987.1:n.*23-405_*23-404insTGGAGTTCTGGGT
NM_000567.3:c.*552_*553insTGGAGTTCTGGGT MANE Select	NP_000558.2:n.*552_*553insTGGAGTTCTGGGT
NM_001329057.2:c.*23-179_*23-178insTGGAGTTCTGGGT	NP_001315986.1:n.*23-179_*23-178insTGGAGTTCTGGGT
NM_001329058.2:c.*23-405_*23-404insTGGAGTTCTGGGT	NP_001315987.1:n.*23-405_*23-404insTGGAGTTCTGGGT
NM_001382703.1:c.*552_*553insTGGAGTTCTGGGT	NP_001369632.1:n.*552_*553insTGGAGTTCTGGGT