Canonical Allele Identifier: CA2610725273

Gene: CYP17A1

Linked Data

• gnomAD v4: 10-102836828-C-CGCCGTATCATTAAAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102836828_102836829insGCCGTATCATTAAAAAA , CM000672.2:g.102836828_102836829insGCCGTATCATTAAAAAA	GRCh38
NC_000010.10:g.104596585_104596586insGCCGTATCATTAAAAAA , CM000672.1:g.104596585_104596586insGCCGTATCATTAAAAAA	GRCh37
NC_000010.9:g.104586575_104586576insGCCGTATCATTAAAAAA	NCBI36
NG_007955.1:g.5705_5706insTTTTTTAATGATACGGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000369887.4:c.297+236_297+237insTTTTTTAATGATACGGC MANE Select	ENSP00000358903.3:n.297+236_297+237insTTTTTTAATGATACGGC
ENST00000638190.1:c.297+236_297+237insTTTTTTAATGATACGGC	ENSP00000492539.1:n.297+236_297+237insTTTTTTAATGATACGGC
ENST00000638272.1:c.297+236_297+237insTTTTTTAATGATACGGC	ENSP00000491508.1:n.297+236_297+237insTTTTTTAATGATACGGC
ENST00000638971.1:c.297+236_297+237insTTTTTTAATGATACGGC	ENSP00000492313.1:n.297+236_297+237insTTTTTTAATGATACGGC
ENST00000639393.1:c.297+236_297+237insTTTTTTAATGATACGGC	ENSP00000492651.1:n.297+236_297+237insTTTTTTAATGATACGGC
ENST00000369887.3:c.297+236_297+237insTTTTTTAATGATACGGC	ENSP00000358903.3:n.297+236_297+237insTTTTTTAATGATACGGC
ENST00000489268.1:n.350+236_350+237insTTTTTTAATGATACGGC
NM_000102.3:c.297+236_297+237insTTTTTTAATGATACGGC	NP_000093.1:n.297+236_297+237insTTTTTTAATGATACGGC
NM_000102.4:c.297+236_297+237insTTTTTTAATGATACGGC MANE Select	NP_000093.1:n.297+236_297+237insTTTTTTAATGATACGGC