Canonical Allele Identifier: CA1932873976
Gene: CYP17A1 HGNC NCBI
CYP17A1-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102834074G= , CM000672.2:g.102834074G= GRCh38
NC_000010.10:g.104593831G= , CM000672.1:g.104593831G= GRCh37
NC_000010.9:g.104583821G= NCBI36
NG_007955.1:g.8460C=

Transcript Alleles

HGVS Amino-acid Change
NM_000102.4:c.715C= (CYP17A1) MANE Select NP_000093.1:p.Arg239=
ENST00000369887.4:c.715C= (CYP17A1) MANE Select ENSP00000358903.3:p.Arg239=
NM_000102.3:c.715C= (CYP17A1) NP_000093.1:p.Arg239=
ENST00000369884.4:n.152-103G=
ENST00000369887.3:c.715C= (CYP17A1) ENSP00000358903.3:p.Arg239=
ENST00000489268.1:n.1631C= (CYP17A1)
ENST00000638190.1:c.666+711C= (CYP17A1) ENSP00000492539.1:n.666+711C=
ENST00000638272.1:c.298-866C= (CYP17A1) ENSP00000491508.1:n.298-866C=
ENST00000638971.1:c.666+711C= (CYP17A1) ENSP00000492313.1:n.666+711C=
ENST00000639393.1:c.715C= (CYP17A1) ENSP00000492651.1:p.Arg239=
ENST00000640633.1:n.477C= (CYP17A1)
XR_428804.1:n.206-103G= (CYP17A1-AS1)