Canonical Allele Identifier: CA3003424118
Gene: CYP17A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102835296del , CM000672.2:g.102835296del GRCh38
NC_000010.10:g.104595053del , CM000672.1:g.104595053del GRCh37
NC_000010.9:g.104585043del NCBI36
NG_007955.1:g.7240del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369887.4:c.396del MANE Select ENSP00000358903.3:p.Phe132LeufsTer?
ENST00000638190.1:c.396del ENSP00000492539.1:p.Phe132LeufsTer?
ENST00000638272.1:c.297+1771del ENSP00000491508.1:n.297+1771del
ENST00000638971.1:c.396del ENSP00000492313.1:p.Phe132LeufsTer?
ENST00000639393.1:c.396del ENSP00000492651.1:p.Phe132LeufsTer?
ENST00000640633.1:n.158del
ENST00000369887.3:c.396del ENSP00000358903.3:p.Phe132LeufsTer?
ENST00000489268.1:n.650del
NM_000102.3:c.396del NP_000093.1:p.Phe132LeufsTer?
NM_000102.4:c.396del MANE Select NP_000093.1:p.Phe132LeufsTer?