Canonical Allele Identifier: CA471287312

Gene: CYP17A1 WBP1L

Linked Data

• MyVariant Identifiers: chr10:g.104590657T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102830900T>A , CM000672.2:g.102830900T>A	GRCh38
NC_000010.10:g.104590657T>A , CM000672.1:g.104590657T>A	GRCh37
NC_000010.9:g.104580647T>A	NCBI36
NG_007955.1:g.11634A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.1329A>T (CYP17A1) MANE Select	ENSP00000358903.3:p.Ile443=
ENST00000638190.1:c.1026A>T (CYP17A1)	ENSP00000492539.1:p.Ile342=
ENST00000638272.1:c.873A>T (CYP17A1)	ENSP00000491508.1:p.Ile291=
ENST00000638971.1:c.1242A>T (CYP17A1)	ENSP00000492313.1:p.Ile414=
ENST00000639393.1:c.1332A>T (CYP17A1)	ENSP00000492651.1:p.Ile444=
ENST00000640633.1:n.1091A>T (CYP17A1)
ENST00000647664.1:c.*582T>A (WBP1L)	ENSP00000498131.1:n.*582T>A
ENST00000369887.3:c.1329A>T (CYP17A1)	ENSP00000358903.3:p.Ile443=
NM_000102.3:c.1329A>T (CYP17A1)	NP_000093.1:p.Ile443=
NM_000102.4:c.1329A>T (CYP17A1) MANE Select	NP_000093.1:p.Ile443=