Canonical Allele Identifier: CA1139772540
Gene: CRP HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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