Canonical Allele Identifier: CA1932870497
Gene: CYP17A1 HGNC NCBI
WBP1L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102832528C= , CM000672.2:g.102832528C= GRCh38
NC_000010.10:g.104592285C= , CM000672.1:g.104592285C= GRCh37
NC_000010.9:g.104582275C= NCBI36
NG_007955.1:g.10006G=

Transcript Alleles

HGVS Amino-acid change
ENST00000369887.4:c.1122G= (CYP17A1) MANE Select ENSP00000358903.3:p.Lys374=
ENST00000638190.1:c.819G= (CYP17A1) ENSP00000492539.1:p.Lys273=
ENST00000638272.1:c.666G= (CYP17A1) ENSP00000491508.1:p.Lys222=
ENST00000638971.1:c.1035G= (CYP17A1) ENSP00000492313.1:p.Lys345=
ENST00000639393.1:c.1122G= (CYP17A1) ENSP00000492651.1:p.Lys374=
ENST00000640633.1:n.884G= (CYP17A1)
ENST00000647664.1:c.*1559C= (WBP1L) ENSP00000498131.1:n.*1559C=
ENST00000369887.3:c.1122G= (CYP17A1) ENSP00000358903.3:p.Lys374=
NM_000102.3:c.1122G= (CYP17A1) NP_000093.1:p.Lys374=
NM_000102.4:c.1122G= (CYP17A1) MANE Select NP_000093.1:p.Lys374=