Canonical Allele Identifier: CA5669481

Gene: CYP17A1 CYP17A1-AS1

Linked Data

• ClinVar Variation Id: 2970583
• ClinVar RCV Id: RCV003824285
• dbSNP Id: rs755207893
• ExAC: 10:104593779 GCT / G
• gnomAD v2: 10-104593779-GCT-G
• gnomAD v4: 10-102834022-GCT-G
• MyVariant Identifiers: chr10:g.104593780_104593781del (hg19) ; chr10:g.102834023_102834024del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102834025_102834026del , CM000672.2:g.102834025_102834026del	GRCh38
NC_000010.10:g.104593782_104593783del , CM000672.1:g.104593782_104593783del	GRCh37
NC_000010.9:g.104583772_104583773del	NCBI36
NG_007955.1:g.8510_8511del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369884.4:n.152-152_152-151del
ENST00000369887.4:c.753+12_753+13del (CYP17A1) MANE Select	ENSP00000358903.3:n.753+12_753+13del
ENST00000638190.1:c.666+761_666+762del (CYP17A1)	ENSP00000492539.1:n.666+761_666+762del
ENST00000638272.1:c.298-816_298-815del (CYP17A1)	ENSP00000491508.1:n.298-816_298-815del
ENST00000638971.1:c.666+761_666+762del (CYP17A1)	ENSP00000492313.1:n.666+761_666+762del
ENST00000639393.1:c.753+12_753+13del (CYP17A1)	ENSP00000492651.1:n.753+12_753+13del
ENST00000640633.1:n.515+12_515+13del (CYP17A1)
ENST00000369887.3:c.753+12_753+13del (CYP17A1)	ENSP00000358903.3:n.753+12_753+13del
ENST00000489268.1:n.1681_1682del (CYP17A1)
NM_000102.3:c.753+12_753+13del (CYP17A1)	NP_000093.1:n.753+12_753+13del
XR_428804.1:n.206-152_206-151del (CYP17A1-AS1)
NM_000102.4:c.753+12_753+13del (CYP17A1) MANE Select	NP_000093.1:n.753+12_753+13del