Canonical Allele Identifier: CA1932866979

Gene: CYP17A1 WBP1L

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102830871A= , CM000672.2:g.102830871A=	GRCh38
NC_000010.10:g.104590628A= , CM000672.1:g.104590628A=	GRCh37
NC_000010.9:g.104580618A=	NCBI36
NG_007955.1:g.11663T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000102.4:c.1358T= (CYP17A1) MANE Select	NP_000093.1:p.Phe453=
ENST00000369887.4:c.1358T= (CYP17A1) MANE Select	ENSP00000358903.3:p.Phe453=
NM_000102.3:c.1358T= (CYP17A1)	NP_000093.1:p.Phe453=
ENST00000369887.3:c.1358T= (CYP17A1)	ENSP00000358903.3:p.Phe453=
ENST00000638190.1:c.1055T= (CYP17A1)	ENSP00000492539.1:p.Phe352=
ENST00000638272.1:c.902T= (CYP17A1)	ENSP00000491508.1:p.Phe301=
ENST00000638971.1:c.1271T= (CYP17A1)	ENSP00000492313.1:p.Phe424=
ENST00000639393.1:c.1361T= (CYP17A1)	ENSP00000492651.1:p.Phe454=
ENST00000640633.1:n.1120T= (CYP17A1)
ENST00000647664.1:c.*553A= (WBP1L)	ENSP00000498131.1:n.*553A=