Canonical Allele Identifier: CA2580581859
Gene: CRP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159712443C>A , CM000663.2:g.159712443C>A GRCh38
NC_000001.10:g.159682233C>A , CM000663.1:g.159682233C>A GRCh37
NC_000001.9:g.157948857C>A NCBI36
NG_013007.1:g.7147G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000255030.9:c.*1082G>T MANE Select ENSP00000255030.5:n.*1082G>T
ENST00000368112.5:c.*374G>T ENSP00000357093.1:n.*374G>T
ENST00000437342.1:c.*374G>T ENSP00000402788.1:n.*374G>T
ENST00000473196.1:n.617G>T
NM_000567.2:c.*1082G>T NP_000558.2:n.*1082G>T
XM_011509207.1:c.*374G>T XP_011507509.1:n.*374G>T
NM_001329057.1:c.*374G>T NP_001315986.1:n.*374G>T
NM_001329058.1:c.*148G>T NP_001315987.1:n.*148G>T
NM_000567.3:c.*1082G>T MANE Select NP_000558.2:n.*1082G>T
NM_001329057.2:c.*374G>T NP_001315986.1:n.*374G>T
NM_001329058.2:c.*148G>T NP_001315987.1:n.*148G>T
NM_001382703.1:c.*1082G>T NP_001369632.1:n.*1082G>T