Canonical Allele Identifier: CA1932873147

Gene: CYP17A1 WBP1L CYP17A1-AS1

Linked Data

• dbSNP Id: rs1844122036
• gnomAD v4: 10-102833678-A-ACT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102833680_102833681dup , CM000672.2:g.102833680_102833681dup	GRCh38
NC_000010.10:g.104593437_104593438dup , CM000672.1:g.104593437_104593438dup	GRCh37
NC_000010.9:g.104583427_104583428dup	NCBI36
NG_007955.1:g.8854_8855dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369884.4:n.152-497_152-496dup
ENST00000369887.4:c.753+356_753+357dup (CYP17A1) MANE Select	ENSP00000358903.3:n.753+356_753+357dup
ENST00000638190.1:c.667-1000_667-999dup (CYP17A1)	ENSP00000492539.1:n.667-1000_667-999dup
ENST00000638272.1:c.298-472_298-471dup (CYP17A1)	ENSP00000491508.1:n.298-472_298-471dup
ENST00000638971.1:c.667-472_667-471dup (CYP17A1)	ENSP00000492313.1:n.667-472_667-471dup
ENST00000639393.1:c.753+356_753+357dup (CYP17A1)	ENSP00000492651.1:n.753+356_753+357dup
ENST00000640633.1:n.515+356_515+357dup (CYP17A1)
ENST00000647664.1:c.*2711_*2712dup (WBP1L)	ENSP00000498131.1:n.*2711_*2712dup
ENST00000369887.3:c.753+356_753+357dup (CYP17A1)	ENSP00000358903.3:n.753+356_753+357dup
ENST00000489268.1:n.2025_2026dup (CYP17A1)
NM_000102.3:c.753+356_753+357dup (CYP17A1)	NP_000093.1:n.753+356_753+357dup
XR_428804.1:n.206-497_206-496dup (CYP17A1-AS1)
NM_000102.4:c.753+356_753+357dup (CYP17A1) MANE Select	NP_000093.1:n.753+356_753+357dup