Canonical Allele Identifier: CA1932841150

Gene: CYP17A1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102837131_102837156delinsGCCGACAATCACTGTAGTCTTGGTGC , CM000672.2:g.102837131_102837156delinsGCCGACAATCACTGTAGTCTTGGTGC	GRCh38
NC_000010.10:g.104596888_104596913delinsGCCGACAATCACTGTAGTCTTGGTGC , CM000672.1:g.104596888_104596913delinsGCCGACAATCACTGTAGTCTTGGTGC	GRCh37
NC_000010.9:g.104586878_104586903delinsGCCGACAATCACTGTAGTCTTGGTGC	NCBI36
NG_007955.1:g.5378_5403delinsGCACCAAGACTACAGTGATTGTCGGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000369887.4:c.206_231delinsGCACCAAGACTACAGTGATTGTCGGC MANE Select	ENSP00000358903.3:p.Gly69=
ENST00000638190.1:c.206_231delinsGCACCAAGACTACAGTGATTGTCGGC	ENSP00000492539.1:p.Gly69=
ENST00000638272.1:c.206_231delinsGCACCAAGACTACAGTGATTGTCGGC	ENSP00000491508.1:p.Gly69=
ENST00000638971.1:c.206_231delinsGCACCAAGACTACAGTGATTGTCGGC	ENSP00000492313.1:p.Gly69=
ENST00000639393.1:c.206_231delinsGCACCAAGACTACAGTGATTGTCGGC	ENSP00000492651.1:p.Gly69=
ENST00000369887.3:c.206_231delinsGCACCAAGACTACAGTGATTGTCGGC	ENSP00000358903.3:p.Gly69=
ENST00000489268.1:n.259_284delinsGCACCAAGACTACAGTGATTGTCGGC
NM_000102.3:c.206_231delinsGCACCAAGACTACAGTGATTGTCGGC	NP_000093.1:p.Gly69=
NM_000102.4:c.206_231delinsGCACCAAGACTACAGTGATTGTCGGC MANE Select	NP_000093.1:p.Gly69=