Canonical Allele Identifier: CA2648593487

Gene: CRP

Linked Data

• gnomAD v4: 1-159713308-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713308A>T , CM000663.2:g.159713308A>T	GRCh38
NC_000001.10:g.159683098A>T , CM000663.1:g.159683098A>T	GRCh37
NC_000001.9:g.157949722A>T	NCBI36
NG_013007.1:g.6282T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000255030.9:c.*217T>A MANE Select	ENSP00000255030.5:n.*217T>A
ENST00000368110.1:c.*22+195T>A	ENSP00000357091.1:n.*22+195T>A
ENST00000368111.5:c.*22+195T>A	ENSP00000357092.1:n.*22+195T>A
ENST00000368112.5:c.*22+195T>A	ENSP00000357093.1:n.*22+195T>A
ENST00000437342.1:c.*22+195T>A	ENSP00000402788.1:n.*22+195T>A
ENST00000473196.1:n.265+195T>A
ENST00000489317.1:n.75-514T>A
NM_000567.2:c.*217T>A	NP_000558.2:n.*217T>A
XM_011509207.1:c.*22+195T>A	XP_011507509.1:n.*22+195T>A
NM_001329057.1:c.*22+195T>A	NP_001315986.1:n.*22+195T>A
NM_001329058.1:c.*22+195T>A	NP_001315987.1:n.*22+195T>A
NM_000567.3:c.*217T>A MANE Select	NP_000558.2:n.*217T>A
NM_001329057.2:c.*22+195T>A	NP_001315986.1:n.*22+195T>A
NM_001329058.2:c.*22+195T>A	NP_001315987.1:n.*22+195T>A
NM_001382703.1:c.*217T>A	NP_001369632.1:n.*217T>A