Canonical Allele Identifier: CA1932873086

Gene: CYP17A1 WBP1L CYP17A1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102833644_102833646delinsCAG , CM000672.2:g.102833644_102833646delinsCAG	GRCh38
NC_000010.10:g.104593401_104593403delinsCAG , CM000672.1:g.104593401_104593403delinsCAG	GRCh37
NC_000010.9:g.104583391_104583393delinsCAG	NCBI36
NG_007955.1:g.8888_8890delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369884.4:n.152-533_152-531delinsCAG
ENST00000369887.4:c.753+390_753+392delinsCTG (CYP17A1) MANE Select	ENSP00000358903.3:n.753+390_753+392delinsCTG
ENST00000638190.1:c.667-966_667-964delinsCTG (CYP17A1)	ENSP00000492539.1:n.667-966_667-964delinsCTG
ENST00000638272.1:c.298-438_298-436delinsCTG (CYP17A1)	ENSP00000491508.1:n.298-438_298-436delinsCTG
ENST00000638971.1:c.667-438_667-436delinsCTG (CYP17A1)	ENSP00000492313.1:n.667-438_667-436delinsCTG
ENST00000639393.1:c.753+390_753+392delinsCTG (CYP17A1)	ENSP00000492651.1:n.753+390_753+392delinsCTG
ENST00000640633.1:n.515+390_515+392delinsCTG (CYP17A1)
ENST00000647664.1:c.*2675_*2677delinsCAG (WBP1L)	ENSP00000498131.1:n.*2675_*2677delinsCAG
ENST00000369887.3:c.753+390_753+392delinsCTG (CYP17A1)	ENSP00000358903.3:n.753+390_753+392delinsCTG
ENST00000489268.1:n.2059_2061delinsCTG (CYP17A1)
NM_000102.3:c.753+390_753+392delinsCTG (CYP17A1)	NP_000093.1:n.753+390_753+392delinsCTG
XR_428804.1:n.206-533_206-531delinsCAG (CYP17A1-AS1)
NM_000102.4:c.753+390_753+392delinsCTG (CYP17A1) MANE Select	NP_000093.1:n.753+390_753+392delinsCTG