Canonical Allele Identifier: CA1468189678
Gene: AFP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73455785C= , CM000666.2:g.73455785C= GRCh38
NC_000004.11:g.74321502C= , CM000666.1:g.74321502C= GRCh37
NC_000004.10:g.74540366C= NCBI36
NG_023028.1:g.24570C=

Transcript Alleles

HGVS Amino-acid change
ENST00000395792.7:c.*165C= MANE Select ENSP00000379138.2:n.*165C=
ENST00000395792.6:c.*165C= ENSP00000379138.2:n.*165C=
NM_001134.2:c.*165C= NP_001125.1:n.*165C=
NM_001354717.1:c.*165C= NP_001341646.1:n.*165C=
NM_001134.3:c.*165C= MANE Select NP_001125.1:n.*165C=
NM_001354717.2:c.*165C= NP_001341646.2:n.*165C=