Canonical Allele Identifier: CA1008297776

Gene: CRP

Linked Data

• gnomAD v3: 1-159712363-T-A
• gnomAD v4: 1-159712363-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159712363T>A , CM000663.2:g.159712363T>A	GRCh38
NC_000001.10:g.159682153T>A , CM000663.1:g.159682153T>A	GRCh37
NC_000001.9:g.157948777T>A	NCBI36
NG_013007.1:g.7227A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.*1162A>T MANE Select	ENSP00000255030.5:n.*1162A>T
ENST00000437342.1:c.*454A>T	ENSP00000402788.1:n.*454A>T
ENST00000473196.1:n.697A>T
NM_000567.2:c.*1162A>T	NP_000558.2:n.*1162A>T
XM_011509207.1:c.*454A>T	XP_011507509.1:n.*454A>T
NM_001329057.1:c.*454A>T	NP_001315986.1:n.*454A>T
NM_001329058.1:c.*228A>T	NP_001315987.1:n.*228A>T
NM_000567.3:c.*1162A>T MANE Select	NP_000558.2:n.*1162A>T
NM_001329057.2:c.*454A>T	NP_001315986.1:n.*454A>T
NM_001329058.2:c.*228A>T	NP_001315987.1:n.*228A>T
NM_001382703.1:c.*1162A>T	NP_001369632.1:n.*1162A>T