Canonical Allele Identifier: CA1008297702

Gene: CRP

Linked Data

• gnomAD v3: 1-159712358-G-GT
• gnomAD v4: 1-159712358-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159712358_159712359insT , CM000663.2:g.159712358_159712359insT	GRCh38
NC_000001.10:g.159682148_159682149insT , CM000663.1:g.159682148_159682149insT	GRCh37
NC_000001.9:g.157948772_157948773insT	NCBI36
NG_013007.1:g.7231_7232insA

Transcript Alleles

HGVS	Amino-acid change
ENST00000255030.9:c.*1166_*1167insA MANE Select	ENSP00000255030.5:n.*1166_*1167insA
ENST00000437342.1:c.*458_*459insA	ENSP00000402788.1:n.*458_*459insA
ENST00000473196.1:n.701_702insA
NM_000567.2:c.*1166_*1167insA	NP_000558.2:n.*1166_*1167insA
XM_011509207.1:c.*458_*459insA	XP_011507509.1:n.*458_*459insA
NM_001329057.1:c.*458_*459insA	NP_001315986.1:n.*458_*459insA
NM_001329058.1:c.*232_*233insA	NP_001315987.1:n.*232_*233insA
NM_000567.3:c.*1166_*1167insA MANE Select	NP_000558.2:n.*1166_*1167insA
NM_001329057.2:c.*458_*459insA	NP_001315986.1:n.*458_*459insA
NM_001329058.2:c.*232_*233insA	NP_001315987.1:n.*232_*233insA
NM_001382703.1:c.*1166_*1167insA	NP_001369632.1:n.*1166_*1167insA