Canonical Allele Identifier: CA2841170166

Gene: CYP17A1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102837330dup , CM000672.2:g.102837330dup	GRCh38
NC_000010.10:g.104597087dup , CM000672.1:g.104597087dup	GRCh37
NC_000010.9:g.104587077dup	NCBI36
NG_007955.1:g.5206dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.34dup MANE Select	ENSP00000358903.3:p.Leu12ProfsTer?
ENST00000638190.1:c.34dup	ENSP00000492539.1:p.Leu12ProfsTer?
ENST00000638272.1:c.34dup	ENSP00000491508.1:p.Leu12ProfsTer?
ENST00000638971.1:c.34dup	ENSP00000492313.1:p.Leu12ProfsTer?
ENST00000639393.1:c.34dup	ENSP00000492651.1:p.Leu12ProfsTer?
ENST00000369887.3:c.34dup	ENSP00000358903.3:p.Leu12ProfsTer?
ENST00000489268.1:n.87dup
NM_000102.3:c.34dup	NP_000093.1:p.Leu12ProfsTer?
NM_000102.4:c.34dup MANE Select	NP_000093.1:p.Leu12ProfsTer?