Canonical Allele Identifier: CA2762178739
Gene: AFP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73455932_73455938del , CM000666.2:g.73455932_73455938del GRCh38
NC_000004.11:g.74321649_74321655del , CM000666.1:g.74321649_74321655del GRCh37
NC_000004.10:g.74540513_74540519del NCBI36
NG_023028.1:g.24717_24723del

Transcript Alleles

HGVS Amino-acid Change
ENST00000395792.7:c.*312_*318del MANE Select ENSP00000379138.2:n.*312_*318del
ENST00000395792.6:c.*312_*318del ENSP00000379138.2:n.*312_*318del
NM_001134.3:c.*312_*318del MANE Select NP_001125.1:n.*312_*318del
NM_001354717.2:c.*312_*318del NP_001341646.2:n.*312_*318del