Canonical Allele Identifier: CA471293217

Gene: CYP17A1 CYP17A1-AS1

Linked Data

• gnomAD v4: 10-102834099-T-C
• MyVariant Identifiers: chr10:g.104593856T>C (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369884.4:n.152-78T>C
ENST00000369887.4:c.690A>G (CYP17A1) MANE Select	ENSP00000358903.3:p.Glu230=
ENST00000638190.1:c.666+686A>G (CYP17A1)	ENSP00000492539.1:n.666+686A>G
ENST00000638272.1:c.298-891A>G (CYP17A1)	ENSP00000491508.1:n.298-891A>G
ENST00000638971.1:c.666+686A>G (CYP17A1)	ENSP00000492313.1:n.666+686A>G
ENST00000639393.1:c.690A>G (CYP17A1)	ENSP00000492651.1:p.Glu230=
ENST00000640633.1:n.452A>G (CYP17A1)
ENST00000369887.3:c.690A>G (CYP17A1)	ENSP00000358903.3:p.Glu230=
ENST00000489268.1:n.1606A>G (CYP17A1)
NM_000102.3:c.690A>G (CYP17A1)	NP_000093.1:p.Glu230=
XR_428804.1:n.206-78T>C (CYP17A1-AS1)
NM_000102.4:c.690A>G (CYP17A1) MANE Select	NP_000093.1:p.Glu230=