Canonical Allele Identifier: CA377938078

Gene: CYP17A1 WBP1L

Linked Data

• gnomAD v4: 10-102830838-T-A
• MyVariant Identifiers: chr10:g.104590595T>A (hg19) ; chr10:g.102830838T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102830838T>A , CM000672.2:g.102830838T>A	GRCh38
NC_000010.10:g.104590595T>A , CM000672.1:g.104590595T>A	GRCh37
NC_000010.9:g.104580585T>A	NCBI36
NG_007955.1:g.11696A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.1391A>T (CYP17A1) MANE Select	ENSP00000358903.3:p.Asp464Val
ENST00000638190.1:c.1088A>T (CYP17A1)	ENSP00000492539.1:p.Asp363Val
ENST00000638272.1:c.935A>T (CYP17A1)	ENSP00000491508.1:p.Asp312Val
ENST00000638971.1:c.1304A>T (CYP17A1)	ENSP00000492313.1:p.Asp435Val
ENST00000639393.1:c.1394A>T (CYP17A1)	ENSP00000492651.1:p.Asp465Val
ENST00000640633.1:n.1153A>T (CYP17A1)
ENST00000647664.1:c.*520T>A (WBP1L)	ENSP00000498131.1:n.*520T>A
ENST00000369887.3:c.1391A>T (CYP17A1)	ENSP00000358903.3:p.Asp464Val
NM_000102.3:c.1391A>T (CYP17A1)	NP_000093.1:p.Asp464Val
NM_000102.4:c.1391A>T (CYP17A1) MANE Select	NP_000093.1:p.Asp464Val