Canonical Allele Identifier: CA2574686301
Gene: CYP17A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102837103_102837105del , CM000672.2:g.102837103_102837105del GRCh38
NC_000010.10:g.104596860_104596862del , CM000672.1:g.104596860_104596862del GRCh37
NC_000010.9:g.104586850_104586852del NCBI36
NG_007955.1:g.5432_5434del

Transcript Alleles

HGVS Amino-acid change
ENST00000369887.4:c.260_262del MANE Select ENSP00000358903.3:p.Ile87del
ENST00000638190.1:c.260_262del ENSP00000492539.1:p.Ile87del
ENST00000638272.1:c.260_262del ENSP00000491508.1:p.Ile87del
ENST00000638971.1:c.260_262del ENSP00000492313.1:p.Ile87del
ENST00000639393.1:c.260_262del ENSP00000492651.1:p.Ile87del
ENST00000369887.3:c.260_262del ENSP00000358903.3:p.Ile87del
ENST00000489268.1:n.313_315del
NM_000102.3:c.260_262del NP_000093.1:p.Ile87del
NM_000102.4:c.260_262del MANE Select NP_000093.1:p.Ile87del