Canonical Allele Identifier: CA5669488

Gene: CYP17A1 CYP17A1-AS1

Linked Data

• ClinVar Variation Id: 2893942
• ClinVar RCV Id: RCV003725553
• dbSNP Id: rs748341718
• ExAC: 10:104593814 A / G
• gnomAD v2: 10-104593814-A-G
• gnomAD v4: 10-102834057-A-G
• MyVariant Identifiers: chr10:g.104593814A>G (hg19) ; chr10:g.102834057A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102834057A>G , CM000672.2:g.102834057A>G	GRCh38
NC_000010.10:g.104593814A>G , CM000672.1:g.104593814A>G	GRCh37
NC_000010.9:g.104583804A>G	NCBI36
NG_007955.1:g.8477T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369884.4:n.152-120A>G
ENST00000369887.4:c.732T>C (CYP17A1) MANE Select	ENSP00000358903.3:p.Asn244=
ENST00000638190.1:c.666+728T>C (CYP17A1)	ENSP00000492539.1:n.666+728T>C
ENST00000638272.1:c.298-849T>C (CYP17A1)	ENSP00000491508.1:n.298-849T>C
ENST00000638971.1:c.666+728T>C (CYP17A1)	ENSP00000492313.1:n.666+728T>C
ENST00000639393.1:c.732T>C (CYP17A1)	ENSP00000492651.1:p.Asn244=
ENST00000640633.1:n.494T>C (CYP17A1)
ENST00000369887.3:c.732T>C (CYP17A1)	ENSP00000358903.3:p.Asn244=
ENST00000489268.1:n.1648T>C (CYP17A1)
NM_000102.3:c.732T>C (CYP17A1)	NP_000093.1:p.Asn244=
XR_428804.1:n.206-120A>G (CYP17A1-AS1)
NM_000102.4:c.732T>C (CYP17A1) MANE Select	NP_000093.1:p.Asn244=