Canonical Allele Identifier: CA377939659

Gene: CYP17A1 CYP17A1-AS1

Linked Data

• MyVariant Identifiers: chr10:g.104593856T>G (hg19) ; chr10:g.102834099T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102834099T>G , CM000672.2:g.102834099T>G	GRCh38
NC_000010.10:g.104593856T>G , CM000672.1:g.104593856T>G	GRCh37
NC_000010.9:g.104583846T>G	NCBI36
NG_007955.1:g.8435A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369884.4:n.152-78T>G
ENST00000369887.4:c.690A>C (CYP17A1) MANE Select	ENSP00000358903.3:p.Glu230Asp
ENST00000638190.1:c.666+686A>C (CYP17A1)	ENSP00000492539.1:n.666+686A>C
ENST00000638272.1:c.298-891A>C (CYP17A1)	ENSP00000491508.1:n.298-891A>C
ENST00000638971.1:c.666+686A>C (CYP17A1)	ENSP00000492313.1:n.666+686A>C
ENST00000639393.1:c.690A>C (CYP17A1)	ENSP00000492651.1:p.Glu230Asp
ENST00000640633.1:n.452A>C (CYP17A1)
ENST00000369887.3:c.690A>C (CYP17A1)	ENSP00000358903.3:p.Glu230Asp
ENST00000489268.1:n.1606A>C (CYP17A1)
NM_000102.3:c.690A>C (CYP17A1)	NP_000093.1:p.Glu230Asp
XR_428804.1:n.206-78T>G (CYP17A1-AS1)
NM_000102.4:c.690A>C (CYP17A1) MANE Select	NP_000093.1:p.Glu230Asp