Canonical Allele Identifier: CA2648592900
Gene: CRP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159712446T>A , CM000663.2:g.159712446T>A GRCh38
NC_000001.10:g.159682236T>A , CM000663.1:g.159682236T>A GRCh37
NC_000001.9:g.157948860T>A NCBI36
NG_013007.1:g.7144A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000255030.9:c.*1079A>T MANE Select ENSP00000255030.5:n.*1079A>T
ENST00000368112.5:c.*371A>T ENSP00000357093.1:n.*371A>T
ENST00000437342.1:c.*371A>T ENSP00000402788.1:n.*371A>T
ENST00000473196.1:n.614A>T
NM_000567.2:c.*1079A>T NP_000558.2:n.*1079A>T
XM_011509207.1:c.*371A>T XP_011507509.1:n.*371A>T
NM_001329057.1:c.*371A>T NP_001315986.1:n.*371A>T
NM_001329058.1:c.*145A>T NP_001315987.1:n.*145A>T
NM_000567.3:c.*1079A>T MANE Select NP_000558.2:n.*1079A>T
NM_001329057.2:c.*371A>T NP_001315986.1:n.*371A>T
NM_001329058.2:c.*145A>T NP_001315987.1:n.*145A>T
NM_001382703.1:c.*1079A>T NP_001369632.1:n.*1079A>T