Canonical Allele Identifier: CA1008297704

Gene: CRP

Linked Data

• gnomAD v3: 1-159712359-C-A
• gnomAD v4: 1-159712359-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159712359C>A , CM000663.2:g.159712359C>A	GRCh38
NC_000001.10:g.159682149C>A , CM000663.1:g.159682149C>A	GRCh37
NC_000001.9:g.157948773C>A	NCBI36
NG_013007.1:g.7231G>T

Transcript Alleles

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