Canonical Allele Identifier: CA2574686215
Gene: CYP17A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102835391del , CM000672.2:g.102835391del GRCh38
NC_000010.10:g.104595148del , CM000672.1:g.104595148del GRCh37
NC_000010.9:g.104585138del NCBI36
NG_007955.1:g.7143del

Transcript Alleles

HGVS Amino-acid change
ENST00000369887.4:c.299del MANE Select ENSP00000358903.3:p.Ala100GlufsTer3
ENST00000638190.1:c.299del ENSP00000492539.1:p.Ala100GlufsTer3
ENST00000638272.1:c.297+1674del ENSP00000491508.1:n.297+1674del
ENST00000638971.1:c.299del ENSP00000492313.1:p.Ala100GlufsTer3
ENST00000639393.1:c.299del ENSP00000492651.1:p.Ala100GlufsTer3
ENST00000640633.1:n.61del
ENST00000369887.3:c.299del ENSP00000358903.3:p.Ala100GlufsTer3
ENST00000489268.1:n.553del
NM_000102.3:c.299del NP_000093.1:p.Ala100GlufsTer3
NM_000102.4:c.299del MANE Select NP_000093.1:p.Ala100GlufsTer3