Canonical Allele Identifier: CA2610723995
Gene: CYP17A1 HGNC NCBI
CYP17A1-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102834102dup , CM000672.2:g.102834102dup GRCh38
NC_000010.10:g.104593859dup , CM000672.1:g.104593859dup GRCh37
NC_000010.9:g.104583849dup NCBI36
NG_007955.1:g.8433dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000369884.4:n.152-75dup
ENST00000369887.4:c.688dup (CYP17A1) MANE Select ENSP00000358903.3:p.Glu230GlyfsTer8
ENST00000638190.1:c.666+684dup (CYP17A1) ENSP00000492539.1:n.666+684dup
ENST00000638272.1:c.298-893dup (CYP17A1) ENSP00000491508.1:n.298-893dup
ENST00000638971.1:c.666+684dup (CYP17A1) ENSP00000492313.1:n.666+684dup
ENST00000639393.1:c.688dup (CYP17A1) ENSP00000492651.1:p.Glu230GlyfsTer8
ENST00000640633.1:n.450dup (CYP17A1)
ENST00000369887.3:c.688dup (CYP17A1) ENSP00000358903.3:p.Glu230GlyfsTer8
ENST00000489268.1:n.1604dup (CYP17A1)
NM_000102.3:c.688dup (CYP17A1) NP_000093.1:p.Glu230GlyfsTer8
XR_428804.1:n.206-75dup (CYP17A1-AS1)
NM_000102.4:c.688dup (CYP17A1) MANE Select NP_000093.1:p.Glu230GlyfsTer8