Canonical Allele Identifier: CA3003421036

Gene: CYP17A1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102837097dup , CM000672.2:g.102837097dup	GRCh38
NC_000010.10:g.104596854dup , CM000672.1:g.104596854dup	GRCh37
NC_000010.9:g.104586844dup	NCBI36
NG_007955.1:g.5438dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.266dup MANE Select	ENSP00000358903.3:p.Lys91GlnfsTer20
ENST00000638190.1:c.266dup	ENSP00000492539.1:p.Lys91GlnfsTer20
ENST00000638272.1:c.266dup	ENSP00000491508.1:p.Lys91GlnfsTer15
ENST00000638971.1:c.266dup	ENSP00000492313.1:p.Lys91GlnfsTer20
ENST00000639393.1:c.266dup	ENSP00000492651.1:p.Lys91GlnfsTer20
ENST00000369887.3:c.266dup	ENSP00000358903.3:p.Lys91GlnfsTer20
ENST00000489268.1:n.319dup
NM_000102.3:c.266dup	NP_000093.1:p.Lys91GlnfsTer20
NM_000102.4:c.266dup MANE Select	NP_000093.1:p.Lys91GlnfsTer20