Canonical Allele Identifier: CA212292884

Gene: CYP17A1 WBP1L CYP17A1-AS1

Linked Data

• dbSNP Id: rs111693081
• gnomAD v4: 10-102833691-GGTGATCTGCCC-G
• MyVariant Identifiers: chr10:g.104593449_104593459del (hg19) ; chr10:g.102833692_102833702del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102833692_102833702del , CM000672.2:g.102833692_102833702del	GRCh38
NC_000010.10:g.104593449_104593459del , CM000672.1:g.104593449_104593459del	GRCh37
NC_000010.9:g.104583439_104583449del	NCBI36
NG_007955.1:g.8832_8842del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369884.4:n.152-485_152-475del
ENST00000369887.4:c.753+334_753+344del (CYP17A1) MANE Select	ENSP00000358903.3:n.753+334_753+344del
ENST00000638190.1:c.667-1022_667-1012del (CYP17A1)	ENSP00000492539.1:n.667-1022_667-1012del
ENST00000638272.1:c.298-494_298-484del (CYP17A1)	ENSP00000491508.1:n.298-494_298-484del
ENST00000638971.1:c.667-494_667-484del (CYP17A1)	ENSP00000492313.1:n.667-494_667-484del
ENST00000639393.1:c.753+334_753+344del (CYP17A1)	ENSP00000492651.1:n.753+334_753+344del
ENST00000640633.1:n.515+334_515+344del (CYP17A1)
ENST00000647664.1:c.*2723_*2733del (WBP1L)	ENSP00000498131.1:n.*2723_*2733del
ENST00000369887.3:c.753+334_753+344del (CYP17A1)	ENSP00000358903.3:n.753+334_753+344del
ENST00000489268.1:n.2003_2013del (CYP17A1)
NM_000102.3:c.753+334_753+344del (CYP17A1)	NP_000093.1:n.753+334_753+344del
XR_428804.1:n.206-485_206-475del (CYP17A1-AS1)
NM_000102.4:c.753+334_753+344del (CYP17A1) MANE Select	NP_000093.1:n.753+334_753+344del