Canonical Allele Identifier: CA1932868293

Gene: CYP17A1 WBP1L

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102831427_102831429delinsCAG , CM000672.2:g.102831427_102831429delinsCAG	GRCh38
NC_000010.10:g.104591184_104591186delinsCAG , CM000672.1:g.104591184_104591186delinsCAG	GRCh37
NC_000010.9:g.104581174_104581176delinsCAG	NCBI36
NG_007955.1:g.11105_11107delinsCTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000369887.4:c.1243+79_1243+81delinsCTG (CYP17A1) MANE Select	ENSP00000358903.3:n.1243+79_1243+81delinsCTG
ENST00000638190.1:c.940+79_940+81delinsCTG (CYP17A1)	ENSP00000492539.1:n.940+79_940+81delinsCTG
ENST00000638272.1:c.787+79_787+81delinsCTG (CYP17A1)	ENSP00000491508.1:n.787+79_787+81delinsCTG
ENST00000638971.1:c.1156+79_1156+81delinsCTG (CYP17A1)	ENSP00000492313.1:n.1156+79_1156+81delinsCTG
ENST00000639393.1:c.1246+79_1246+81delinsCTG (CYP17A1)	ENSP00000492651.1:n.1246+79_1246+81delinsCTG
ENST00000640633.1:n.1005+79_1005+81delinsCTG (CYP17A1)
ENST00000647664.1:c.*629-171_*629-169delinsCAG (WBP1L)	ENSP00000498131.1:n.*629-171_*629-169delinsCAG
ENST00000369887.3:c.1243+79_1243+81delinsCTG (CYP17A1)	ENSP00000358903.3:n.1243+79_1243+81delinsCTG
ENST00000469683.1:n.196+79_196+81delinsCTG (CYP17A1)
NM_000102.3:c.1243+79_1243+81delinsCTG (CYP17A1)	NP_000093.1:n.1243+79_1243+81delinsCTG
NM_000102.4:c.1243+79_1243+81delinsCTG (CYP17A1) MANE Select	NP_000093.1:n.1243+79_1243+81delinsCTG