Canonical Allele Identifier: CA1932841076
Gene: CYP17A1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102837073_102837074delinsGC , CM000672.2:g.102837073_102837074delinsGC GRCh38
NC_000010.10:g.104596830_104596831delinsGC , CM000672.1:g.104596830_104596831delinsGC GRCh37
NC_000010.9:g.104586820_104586821delinsGC NCBI36
NG_007955.1:g.5460_5461delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000369887.4:c.288_289delinsGC MANE Select ENSP00000358903.3:p.Arg96=
ENST00000638190.1:c.288_289delinsGC ENSP00000492539.1:p.Arg96=
ENST00000638272.1:c.288_289delinsGC ENSP00000491508.1:p.Arg96=
ENST00000638971.1:c.288_289delinsGC ENSP00000492313.1:p.Arg96=
ENST00000639393.1:c.288_289delinsGC ENSP00000492651.1:p.Arg96=
ENST00000369887.3:c.288_289delinsGC ENSP00000358903.3:p.Arg96=
ENST00000489268.1:n.341_342delinsGC
NM_000102.3:c.288_289delinsGC NP_000093.1:p.Arg96=
NM_000102.4:c.288_289delinsGC MANE Select NP_000093.1:p.Arg96=
Search 100 bp 5'
Search 100 bp 3'