Canonical Allele Identifier: CA343454364
Gene: CRP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159713880A>T , CM000663.2:g.159713880A>T GRCh38
NC_000001.10:g.159683670A>T , CM000663.1:g.159683670A>T GRCh37
NC_000001.9:g.157950294A>T NCBI36
NG_013007.1:g.5710T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000255030.9:c.320T>A MANE Select ENSP00000255030.5:p.Val107Asp
ENST00000368110.1:c.193+127T>A ENSP00000357091.1:n.193+127T>A
ENST00000368111.5:c.193+127T>A ENSP00000357092.1:n.193+127T>A
ENST00000368112.5:c.197+123T>A ENSP00000357093.1:n.197+123T>A
ENST00000437342.1:c.-215T>A ENSP00000402788.1:n.-215T>A
ENST00000489317.1:n.74+127T>A
NM_000567.2:c.320T>A NP_000558.2:p.Val107Asp
XM_011509207.1:c.320T>A XP_011507509.1:p.Val107Asp
NM_001329057.1:c.320T>A NP_001315986.1:p.Val107Asp
NM_001329058.1:c.197+123T>A NP_001315987.1:n.197+123T>A
NM_000567.3:c.320T>A MANE Select NP_000558.2:p.Val107Asp
NM_001329057.2:c.320T>A NP_001315986.1:p.Val107Asp
NM_001329058.2:c.197+123T>A NP_001315987.1:n.197+123T>A
NM_001382703.1:c.193+127T>A NP_001369632.1:n.193+127T>A