Canonical Allele Identifier: CA2648592921
Gene: CRP HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

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