Canonical Allele Identifier: CA2648592775

Gene: CRP

Linked Data

• gnomAD v4: 1-159712361-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159712361_159712362insT , CM000663.2:g.159712361_159712362insT	GRCh38
NC_000001.10:g.159682151_159682152insT , CM000663.1:g.159682151_159682152insT	GRCh37
NC_000001.9:g.157948775_157948776insT	NCBI36
NG_013007.1:g.7228_7229insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.*1163_*1164insA MANE Select	ENSP00000255030.5:n.*1163_*1164insA
ENST00000437342.1:c.*455_*456insA	ENSP00000402788.1:n.*455_*456insA
ENST00000473196.1:n.698_699insA
NM_000567.2:c.*1163_*1164insA	NP_000558.2:n.*1163_*1164insA
XM_011509207.1:c.*455_*456insA	XP_011507509.1:n.*455_*456insA
NM_001329057.1:c.*455_*456insA	NP_001315986.1:n.*455_*456insA
NM_001329058.1:c.*229_*230insA	NP_001315987.1:n.*229_*230insA
NM_000567.3:c.*1163_*1164insA MANE Select	NP_000558.2:n.*1163_*1164insA
NM_001329057.2:c.*455_*456insA	NP_001315986.1:n.*455_*456insA
NM_001329058.2:c.*229_*230insA	NP_001315987.1:n.*229_*230insA
NM_001382703.1:c.*1163_*1164insA	NP_001369632.1:n.*1163_*1164insA