Canonical Allele Identifier: CA2574686211
Gene: CYP17A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102835377_102835378del , CM000672.2:g.102835377_102835378del GRCh38
NC_000010.10:g.104595134_104595135del , CM000672.1:g.104595134_104595135del GRCh37
NC_000010.9:g.104585124_104585125del NCBI36
NG_007955.1:g.7158_7159del

Transcript Alleles

HGVS Amino-acid change
ENST00000369887.4:c.314_315del MANE Select ENSP00000358903.3:p.Ala105ValfsTer5
ENST00000638190.1:c.314_315del ENSP00000492539.1:p.Ala105ValfsTer5
ENST00000638272.1:c.297+1689_297+1690del ENSP00000491508.1:n.297+1689_297+1690del
ENST00000638971.1:c.314_315del ENSP00000492313.1:p.Ala105ValfsTer5
ENST00000639393.1:c.314_315del ENSP00000492651.1:p.Ala105ValfsTer5
ENST00000640633.1:n.76_77del
ENST00000369887.3:c.314_315del ENSP00000358903.3:p.Ala105ValfsTer5
ENST00000489268.1:n.568_569del
NM_000102.3:c.314_315del NP_000093.1:p.Ala105ValfsTer5
NM_000102.4:c.314_315del MANE Select NP_000093.1:p.Ala105ValfsTer5