Canonical Allele Identifier: CA212292874

Gene: CYP17A1 WBP1L CYP17A1-AS1

Linked Data

• dbSNP Id: rs985385165
• gnomAD v3: 10-102833647-AGTTTCTC-A
• gnomAD v4: 10-102833647-AGTTTCTC-A
• MyVariant Identifiers: chr10:g.104593405_104593411del (hg19) ; chr10:g.102833648_102833654del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102833648_102833654del , CM000672.2:g.102833648_102833654del	GRCh38
NC_000010.10:g.104593405_104593411del , CM000672.1:g.104593405_104593411del	GRCh37
NC_000010.9:g.104583395_104583401del	NCBI36
NG_007955.1:g.8880_8886del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369884.4:n.152-529_152-523del
ENST00000369887.4:c.753+382_753+388del (CYP17A1) MANE Select	ENSP00000358903.3:n.753+382_753+388del
ENST00000638190.1:c.667-974_667-968del (CYP17A1)	ENSP00000492539.1:n.667-974_667-968del
ENST00000638272.1:c.298-446_298-440del (CYP17A1)	ENSP00000491508.1:n.298-446_298-440del
ENST00000638971.1:c.667-446_667-440del (CYP17A1)	ENSP00000492313.1:n.667-446_667-440del
ENST00000639393.1:c.753+382_753+388del (CYP17A1)	ENSP00000492651.1:n.753+382_753+388del
ENST00000640633.1:n.515+382_515+388del (CYP17A1)
ENST00000647664.1:c.*2679_*2685del (WBP1L)	ENSP00000498131.1:n.*2679_*2685del
ENST00000369887.3:c.753+382_753+388del (CYP17A1)	ENSP00000358903.3:n.753+382_753+388del
ENST00000489268.1:n.2051_2057del (CYP17A1)
NM_000102.3:c.753+382_753+388del (CYP17A1)	NP_000093.1:n.753+382_753+388del
XR_428804.1:n.206-529_206-523del (CYP17A1-AS1)
NM_000102.4:c.753+382_753+388del (CYP17A1) MANE Select	NP_000093.1:n.753+382_753+388del