Canonical Allele Identifier: CA343454252
Gene: CRP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159713824C>T , CM000663.2:g.159713824C>T GRCh38
NC_000001.10:g.159683614C>T , CM000663.1:g.159683614C>T GRCh37
NC_000001.9:g.157950238C>T NCBI36
NG_013007.1:g.5766G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000255030.9:c.376G>A MANE Select ENSP00000255030.5:p.Glu126Lys
ENST00000368110.1:c.194-184G>A ENSP00000357091.1:n.194-184G>A
ENST00000368111.5:c.194-184G>A ENSP00000357092.1:n.194-184G>A
ENST00000368112.5:c.197+179G>A ENSP00000357093.1:n.197+179G>A
ENST00000437342.1:c.-159G>A ENSP00000402788.1:n.-159G>A
ENST00000489317.1:n.74+183G>A
NM_000567.2:c.376G>A NP_000558.2:p.Glu126Lys
XM_011509207.1:c.376G>A XP_011507509.1:p.Glu126Lys
NM_001329057.1:c.376G>A NP_001315986.1:p.Glu126Lys
NM_001329058.1:c.197+179G>A NP_001315987.1:n.197+179G>A
NM_000567.3:c.376G>A MANE Select NP_000558.2:p.Glu126Lys
NM_001329057.2:c.376G>A NP_001315986.1:p.Glu126Lys
NM_001329058.2:c.197+179G>A NP_001315987.1:n.197+179G>A
NM_001382703.1:c.194-184G>A NP_001369632.1:n.194-184G>A