Canonical Allele Identifier: CA1932873719
Gene: CYP17A1 HGNC NCBI
CYP17A1-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102833985C= , CM000672.2:g.102833985C= GRCh38
NC_000010.10:g.104593742C= , CM000672.1:g.104593742C= GRCh37
NC_000010.9:g.104583732C= NCBI36
NG_007955.1:g.8549G=

Transcript Alleles

HGVS Amino-acid change
ENST00000369884.4:n.152-192C=
ENST00000369887.4:c.753+51G= (CYP17A1) MANE Select ENSP00000358903.3:n.753+51G=
ENST00000638190.1:c.666+800G= (CYP17A1) ENSP00000492539.1:n.666+800G=
ENST00000638272.1:c.298-777G= (CYP17A1) ENSP00000491508.1:n.298-777G=
ENST00000638971.1:c.667-777G= (CYP17A1) ENSP00000492313.1:n.667-777G=
ENST00000639393.1:c.753+51G= (CYP17A1) ENSP00000492651.1:n.753+51G=
ENST00000640633.1:n.515+51G= (CYP17A1)
ENST00000369887.3:c.753+51G= (CYP17A1) ENSP00000358903.3:n.753+51G=
ENST00000489268.1:n.1720G= (CYP17A1)
NM_000102.3:c.753+51G= (CYP17A1) NP_000093.1:n.753+51G=
XR_428804.1:n.206-192C= (CYP17A1-AS1)
NM_000102.4:c.753+51G= (CYP17A1) MANE Select NP_000093.1:n.753+51G=