Canonical Allele Identifier: CA1008297692

Gene: CRP

Linked Data

• gnomAD v3: 1-159712353-A-AT
• gnomAD v4: 1-159712353-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159712353_159712354insT , CM000663.2:g.159712353_159712354insT	GRCh38
NC_000001.10:g.159682143_159682144insT , CM000663.1:g.159682143_159682144insT	GRCh37
NC_000001.9:g.157948767_157948768insT	NCBI36
NG_013007.1:g.7236_7237insA

Transcript Alleles

HGVS	Amino-acid change
ENST00000255030.9:c.*1171_*1172insA MANE Select	ENSP00000255030.5:n.*1171_*1172insA
ENST00000437342.1:c.*463_*464insA	ENSP00000402788.1:n.*463_*464insA
ENST00000473196.1:n.706_707insA
NM_000567.2:c.*1171_*1172insA	NP_000558.2:n.*1171_*1172insA
XM_011509207.1:c.*463_*464insA	XP_011507509.1:n.*463_*464insA
NM_001329057.1:c.*463_*464insA	NP_001315986.1:n.*463_*464insA
NM_001329058.1:c.*237_*238insA	NP_001315987.1:n.*237_*238insA
NM_000567.3:c.*1171_*1172insA MANE Select	NP_000558.2:n.*1171_*1172insA
NM_001329057.2:c.*463_*464insA	NP_001315986.1:n.*463_*464insA
NM_001329058.2:c.*237_*238insA	NP_001315987.1:n.*237_*238insA
NM_001382703.1:c.*1171_*1172insA	NP_001369632.1:n.*1171_*1172insA