Canonical Allele Identifier: CA212293088

Gene: CYP17A1 CYP17A1-AS1

Linked Data

• ClinVar Variation Id: 1193245
• ClinVar RCV Id: RCV001555585
• dbSNP Id: rs148246693
• gnomAD v2: 10-104593638-C-A
• gnomAD v3: 10-102833881-C-A
• gnomAD v4: 10-102833881-C-A
• MyVariant Identifiers: chr10:g.104593638C>A (hg19) ; chr10:g.102833881C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102833881C>A , CM000672.2:g.102833881C>A	GRCh38
NC_000010.10:g.104593638C>A , CM000672.1:g.104593638C>A	GRCh37
NC_000010.9:g.104583628C>A	NCBI36
NG_007955.1:g.8653G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369884.4:n.152-296C>A
ENST00000369887.4:c.753+155G>T (CYP17A1) MANE Select	ENSP00000358903.3:n.753+155G>T
ENST00000638190.1:c.666+904G>T (CYP17A1)	ENSP00000492539.1:n.666+904G>T
ENST00000638272.1:c.298-673G>T (CYP17A1)	ENSP00000491508.1:n.298-673G>T
ENST00000638971.1:c.667-673G>T (CYP17A1)	ENSP00000492313.1:n.667-673G>T
ENST00000639393.1:c.753+155G>T (CYP17A1)	ENSP00000492651.1:n.753+155G>T
ENST00000640633.1:n.515+155G>T (CYP17A1)
ENST00000369887.3:c.753+155G>T (CYP17A1)	ENSP00000358903.3:n.753+155G>T
ENST00000489268.1:n.1824G>T (CYP17A1)
NM_000102.3:c.753+155G>T (CYP17A1)	NP_000093.1:n.753+155G>T
XR_428804.1:n.206-296C>A (CYP17A1-AS1)
NM_000102.4:c.753+155G>T (CYP17A1) MANE Select	NP_000093.1:n.753+155G>T