Canonical Allele Identifier: CA1932841042

Gene: CYP17A1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102837041_102837042delinsAG , CM000672.2:g.102837041_102837042delinsAG	GRCh38
NC_000010.10:g.104596798_104596799delinsAG , CM000672.1:g.104596798_104596799delinsAG	GRCh37
NC_000010.9:g.104586788_104586789delinsAG	NCBI36
NG_007955.1:g.5492_5493delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000369887.4:c.297+23_297+24delinsCT MANE Select	ENSP00000358903.3:n.297+23_297+24delinsCT...
ENST00000638190.1:c.297+23_297+24delinsCT	ENSP00000492539.1:n.297+23_297+24delinsCT...
ENST00000638272.1:c.297+23_297+24delinsCT	ENSP00000491508.1:n.297+23_297+24delinsCT...
ENST00000638971.1:c.297+23_297+24delinsCT	ENSP00000492313.1:n.297+23_297+24delinsCT...
ENST00000639393.1:c.297+23_297+24delinsCT	ENSP00000492651.1:n.297+23_297+24delinsCT...
ENST00000369887.3:c.297+23_297+24delinsCT	ENSP00000358903.3:n.297+23_297+24delinsCT...
ENST00000489268.1:n.350+23_350+24delinsCT
NM_000102.3:c.297+23_297+24delinsCT	NP_000093.1:n.297+23_297+24delinsCT
NM_000102.4:c.297+23_297+24delinsCT MANE Select	NP_000093.1:n.297+23_297+24delinsCT