Canonical Allele Identifier: CA377939635

Gene: CYP17A1 CYP17A1-AS1

Linked Data

• gnomAD v4: 10-102834089-T-A
• MyVariant Identifiers: chr10:g.104593846T>A (hg19) ; chr10:g.102834089T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102834089T>A , CM000672.2:g.102834089T>A	GRCh38
NC_000010.10:g.104593846T>A , CM000672.1:g.104593846T>A	GRCh37
NC_000010.9:g.104583836T>A	NCBI36
NG_007955.1:g.8445A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369884.4:n.152-88T>A
ENST00000369887.4:c.700A>T (CYP17A1) MANE Select	ENSP00000358903.3:p.Ser234Cys
ENST00000638190.1:c.666+696A>T (CYP17A1)	ENSP00000492539.1:n.666+696A>T
ENST00000638272.1:c.298-881A>T (CYP17A1)	ENSP00000491508.1:n.298-881A>T
ENST00000638971.1:c.666+696A>T (CYP17A1)	ENSP00000492313.1:n.666+696A>T
ENST00000639393.1:c.700A>T (CYP17A1)	ENSP00000492651.1:p.Ser234Cys
ENST00000640633.1:n.462A>T (CYP17A1)
ENST00000369887.3:c.700A>T (CYP17A1)	ENSP00000358903.3:p.Ser234Cys
ENST00000489268.1:n.1616A>T (CYP17A1)
NM_000102.3:c.700A>T (CYP17A1)	NP_000093.1:p.Ser234Cys
XR_428804.1:n.206-88T>A (CYP17A1-AS1)
NM_000102.4:c.700A>T (CYP17A1) MANE Select	NP_000093.1:p.Ser234Cys