Canonical Allele Identifier: CA2695203410

Gene: CYP17A1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102835298del , CM000672.2:g.102835298del	GRCh38
NC_000010.10:g.104595055del , CM000672.1:g.104595055del	GRCh37
NC_000010.9:g.104585045del	NCBI36
NG_007955.1:g.7237del

Transcript Alleles

HGVS	Amino-acid change
ENST00000369887.4:c.393del MANE Select	ENSP00000358903.3:p.Phe132LeufsTer?
ENST00000638190.1:c.393del	ENSP00000492539.1:p.Phe132LeufsTer?
ENST00000638272.1:c.297+1768del	ENSP00000491508.1:n.297+1768del
ENST00000638971.1:c.393del	ENSP00000492313.1:p.Phe132LeufsTer?
ENST00000639393.1:c.393del	ENSP00000492651.1:p.Phe132LeufsTer?
ENST00000640633.1:n.155del
ENST00000369887.3:c.393del	ENSP00000358903.3:p.Phe132LeufsTer?
ENST00000489268.1:n.647del
NM_000102.3:c.393del	NP_000093.1:p.Phe132LeufsTer?
NM_000102.4:c.393del MANE Select	NP_000093.1:p.Phe132LeufsTer?