Canonical Allele Identifier: CA5669311

Gene: CYP17A1 WBP1L

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102830742C>T , CM000672.2:g.102830742C>T	GRCh38
NC_000010.10:g.104590499C>T , CM000672.1:g.104590499C>T	GRCh37
NC_000010.9:g.104580489C>T	NCBI36
NG_007955.1:g.11792G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000102.4:c.1487G>A (CYP17A1) MANE Select	NP_000093.1:p.Arg496His
ENST00000369887.4:c.1487G>A (CYP17A1) MANE Select	ENSP00000358903.3:p.Arg496His
NM_000102.3:c.1487G>A (CYP17A1)	NP_000093.1:p.Arg496His
ENST00000369887.3:c.1487G>A (CYP17A1)	ENSP00000358903.3:p.Arg496His
ENST00000638190.1:c.1184G>A (CYP17A1)	ENSP00000492539.1:p.Arg395His
ENST00000638272.1:c.1031G>A (CYP17A1)	ENSP00000491508.1:p.Arg344His
ENST00000638971.1:c.1400G>A (CYP17A1)	ENSP00000492313.1:p.Arg467His
ENST00000639393.1:c.1490G>A (CYP17A1)	ENSP00000492651.1:p.Arg497His
ENST00000640633.1:n.1249G>A (CYP17A1)
ENST00000647664.1:c.*424C>T (WBP1L)	ENSP00000498131.1:n.*424C>T