Canonical Allele Identifier: CA343453447
Gene: CRP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159713556T>C , CM000663.2:g.159713556T>C GRCh38
NC_000001.10:g.159683346T>C , CM000663.1:g.159683346T>C GRCh37
NC_000001.9:g.157949970T>C NCBI36
NG_013007.1:g.6034A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000255030.9:c.644A>G MANE Select ENSP00000255030.5:p.Glu215Gly
ENST00000368110.1:c.278A>G ENSP00000357091.1:p.Glu93Gly
ENST00000368111.5:c.278A>G ENSP00000357092.1:p.Glu93Gly
ENST00000368112.5:c.245A>G ENSP00000357093.1:p.Glu82Gly
ENST00000437342.1:c.110A>G ENSP00000402788.1:p.Glu37Gly
ENST00000473196.1:n.212A>G
ENST00000489317.1:n.74+451A>G
NM_000567.2:c.644A>G NP_000558.2:p.Glu215Gly
XM_011509207.1:c.644A>G XP_011507509.1:p.Glu215Gly
NM_001329057.1:c.644A>G NP_001315986.1:p.Glu215Gly
NM_001329058.1:c.245A>G NP_001315987.1:p.Glu82Gly
NM_000567.3:c.644A>G MANE Select NP_000558.2:p.Glu215Gly
NM_001329057.2:c.644A>G NP_001315986.1:p.Glu215Gly
NM_001329058.2:c.245A>G NP_001315987.1:p.Glu82Gly
NM_001382703.1:c.278A>G NP_001369632.1:p.Glu93Gly