Canonical Allele Identifier: CA931952449

Gene: CYP17A1 CYP17A1-AS1

Linked Data

• dbSNP Id: rs1844124515
• gnomAD v3: 10-102833915-CCTA-C
• gnomAD v4: 10-102833915-CCTA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102833919_102833921del , CM000672.2:g.102833919_102833921del	GRCh38
NC_000010.10:g.104593676_104593678del , CM000672.1:g.104593676_104593678del	GRCh37
NC_000010.9:g.104583666_104583668del	NCBI36
NG_007955.1:g.8616_8618del

Transcript Alleles

HGVS	Amino-acid change
ENST00000369884.4:n.152-258_152-256del
ENST00000369887.4:c.753+118_753+120del (CYP17A1) MANE Select	ENSP00000358903.3:n.753+118_753+120del
ENST00000638190.1:c.666+867_666+869del (CYP17A1)	ENSP00000492539.1:n.666+867_666+869del
ENST00000638272.1:c.298-710_298-708del (CYP17A1)	ENSP00000491508.1:n.298-710_298-708del
ENST00000638971.1:c.667-710_667-708del (CYP17A1)	ENSP00000492313.1:n.667-710_667-708del
ENST00000639393.1:c.753+118_753+120del (CYP17A1)	ENSP00000492651.1:n.753+118_753+120del
ENST00000640633.1:n.515+118_515+120del (CYP17A1)
ENST00000369887.3:c.753+118_753+120del (CYP17A1)	ENSP00000358903.3:n.753+118_753+120del
ENST00000489268.1:n.1787_1789del (CYP17A1)
NM_000102.3:c.753+118_753+120del (CYP17A1)	NP_000093.1:n.753+118_753+120del
XR_428804.1:n.206-258_206-256del (CYP17A1-AS1)
NM_000102.4:c.753+118_753+120del (CYP17A1) MANE Select	NP_000093.1:n.753+118_753+120del