Canonical Allele Identifier: CA1932870617
Gene: CYP17A1 HGNC NCBI
WBP1L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102832577C= , CM000672.2:g.102832577C= GRCh38
NC_000010.10:g.104592334C= , CM000672.1:g.104592334C= GRCh37
NC_000010.9:g.104582324C= NCBI36
NG_007955.1:g.9957G=

Transcript Alleles

HGVS Amino-acid Change
NM_000102.4:c.1073G= (CYP17A1) MANE Select NP_000093.1:p.Arg358=
ENST00000369887.4:c.1073G= (CYP17A1) MANE Select ENSP00000358903.3:p.Arg358=
NM_000102.3:c.1073G= (CYP17A1) NP_000093.1:p.Arg358=
ENST00000369887.3:c.1073G= (CYP17A1) ENSP00000358903.3:p.Arg358=
ENST00000638190.1:c.770G= (CYP17A1) ENSP00000492539.1:p.Arg257=
ENST00000638272.1:c.617G= (CYP17A1) ENSP00000491508.1:p.Arg206=
ENST00000638971.1:c.986G= (CYP17A1) ENSP00000492313.1:p.Arg329=
ENST00000639393.1:c.1073G= (CYP17A1) ENSP00000492651.1:p.Arg358=
ENST00000640633.1:n.835G= (CYP17A1)
ENST00000647664.1:c.*1608C= (WBP1L) ENSP00000498131.1:n.*1608C=