Canonical Allele Identifier: CA471288759

Gene: CYP17A1 WBP1L

Linked Data

• MyVariant Identifiers: chr10:g.104592405C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102832648C>T , CM000672.2:g.102832648C>T	GRCh38
NC_000010.10:g.104592405C>T , CM000672.1:g.104592405C>T	GRCh37
NC_000010.9:g.104582395C>T	NCBI36
NG_007955.1:g.9886G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.1002G>A (CYP17A1) MANE Select	ENSP00000358903.3:p.Gln334=
ENST00000638190.1:c.699G>A (CYP17A1)	ENSP00000492539.1:p.Gln233=
ENST00000638272.1:c.546G>A (CYP17A1)	ENSP00000491508.1:p.Gln182=
ENST00000638971.1:c.915G>A (CYP17A1)	ENSP00000492313.1:p.Gln305=
ENST00000639393.1:c.1002G>A (CYP17A1)	ENSP00000492651.1:p.Gln334=
ENST00000640633.1:n.764G>A (CYP17A1)
ENST00000647664.1:c.*1679C>T (WBP1L)	ENSP00000498131.1:n.*1679C>T
ENST00000369887.3:c.1002G>A (CYP17A1)	ENSP00000358903.3:p.Gln334=
NM_000102.3:c.1002G>A (CYP17A1)	NP_000093.1:p.Gln334=
NM_000102.4:c.1002G>A (CYP17A1) MANE Select	NP_000093.1:p.Gln334=