Canonical Allele Identifier: CA1932867592

Gene: CYP17A1 WBP1L

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102831085C= , CM000672.2:g.102831085C=	GRCh38
NC_000010.10:g.104590842C= , CM000672.1:g.104590842C=	GRCh37
NC_000010.9:g.104580832C=	NCBI36
NG_007955.1:g.11449G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.1244-100G= (CYP17A1) MANE Select	ENSP00000358903.3:n.1244-100G=
ENST00000638190.1:c.941-100G= (CYP17A1)	ENSP00000492539.1:n.941-100G=
ENST00000638272.1:c.788-100G= (CYP17A1)	ENSP00000491508.1:n.788-100G=
ENST00000638971.1:c.1157-100G= (CYP17A1)	ENSP00000492313.1:n.1157-100G=
ENST00000639393.1:c.1247-100G= (CYP17A1)	ENSP00000492651.1:n.1247-100G=
ENST00000640633.1:n.1006-100G= (CYP17A1)
ENST00000647664.1:c.*628+139C= (WBP1L)	ENSP00000498131.1:n.*628+139C=
ENST00000369887.3:c.1244-100G= (CYP17A1)	ENSP00000358903.3:n.1244-100G=
ENST00000469683.1:n.197-100G= (CYP17A1)
NM_000102.3:c.1244-100G= (CYP17A1)	NP_000093.1:n.1244-100G=
NM_000102.4:c.1244-100G= (CYP17A1) MANE Select	NP_000093.1:n.1244-100G=