Canonical Allele Identifier: CA2648592922

Gene: CRP

Linked Data

• gnomAD v4: 1-159712459-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159712459G>T , CM000663.2:g.159712459G>T	GRCh38
NC_000001.10:g.159682249G>T , CM000663.1:g.159682249G>T	GRCh37
NC_000001.9:g.157948873G>T	NCBI36
NG_013007.1:g.7131C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000255030.9:c.*1066C>A MANE Select	ENSP00000255030.5:n.*1066C>A
ENST00000368112.5:c.*358C>A	ENSP00000357093.1:n.*358C>A
ENST00000437342.1:c.*358C>A	ENSP00000402788.1:n.*358C>A
ENST00000473196.1:n.601C>A
NM_000567.2:c.*1066C>A	NP_000558.2:n.*1066C>A
XM_011509207.1:c.*358C>A	XP_011507509.1:n.*358C>A
NM_001329057.1:c.*358C>A	NP_001315986.1:n.*358C>A
NM_001329058.1:c.*132C>A	NP_001315987.1:n.*132C>A
NM_000567.3:c.*1066C>A MANE Select	NP_000558.2:n.*1066C>A
NM_001329057.2:c.*358C>A	NP_001315986.1:n.*358C>A
NM_001329058.2:c.*132C>A	NP_001315987.1:n.*132C>A
NM_001382703.1:c.*1066C>A	NP_001369632.1:n.*1066C>A