Canonical Allele Identifier: CA2648592766

Gene: CRP

Linked Data

• gnomAD v4: 1-159712359-CTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159712360_159712361del , CM000663.2:g.159712360_159712361del	GRCh38
NC_000001.10:g.159682150_159682151del , CM000663.1:g.159682150_159682151del	GRCh37
NC_000001.9:g.157948774_157948775del	NCBI36
NG_013007.1:g.7229_7230del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.*1164_*1165del MANE Select	ENSP00000255030.5:n.*1164_*1165del
ENST00000437342.1:c.*456_*457del	ENSP00000402788.1:n.*456_*457del
ENST00000473196.1:n.699_700del
NM_000567.2:c.*1164_*1165del	NP_000558.2:n.*1164_*1165del
XM_011509207.1:c.*456_*457del	XP_011507509.1:n.*456_*457del
NM_001329057.1:c.*456_*457del	NP_001315986.1:n.*456_*457del
NM_001329058.1:c.*230_*231del	NP_001315987.1:n.*230_*231del
NM_000567.3:c.*1164_*1165del MANE Select	NP_000558.2:n.*1164_*1165del
NM_001329057.2:c.*456_*457del	NP_001315986.1:n.*456_*457del
NM_001329058.2:c.*230_*231del	NP_001315987.1:n.*230_*231del
NM_001382703.1:c.*1164_*1165del	NP_001369632.1:n.*1164_*1165del