Canonical Allele Identifier: CA2569143601
Gene: CYP17A1 HGNC NCBI
WBP1L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102831435_102831436insTACCCGTCACTGAAGTGGATGAAAAGAGCTTTTATCGTCAGCAGGAAGCTGTCATTCGGGAGATGACAAAACTCAGTTGATAGCATAAATCCCGTGCTGTCTTTCTGTAGGTAAGCACAGTTAAGTTCTC , CM000672.2:g.102831435_102831436insTACCCGTCACTGAAGTGGATGAAAAGAGCTTTTATCGTCAGCAGGAAGCTGTCATTCGGGAGATGACAAAACTCAGTTGATAGCATAAATCCCGTGCTGTCTTTCTGTAGGTAAGCACAGTTAAGTTCTC GRCh38
NC_000010.10:g.104591192_104591193insTACCCGTCACTGAAGTGGATGAAAAGAGCTTTTATCGTCAGCAGGAAGCTGTCATTCGGGAGATGACAAAACTCAGTTGATAGCATAAATCCCGTGCTGTCTTTCTGTAGGTAAGCACAGTTAAGTTCTC , CM000672.1:g.104591192_104591193insTACCCGTCACTGAAGTGGATGAAAAGAGCTTTTATCGTCAGCAGGAAGCTGTCATTCGGGAGATGACAAAACTCAGTTGATAGCATAAATCCCGTGCTGTCTTTCTGTAGGTAAGCACAGTTAAGTTCTC GRCh37
NC_000010.9:g.104581182_104581183insTACCCGTCACTGAAGTGGATGAAAAGAGCTTTTATCGTCAGCAGGAAGCTGTCATTCGGGAGATGACAAAACTCAGTTGATAGCATAAATCCCGTGCTGTCTTTCTGTAGGTAAGCACAGTTAAGTTCTC NCBI36
NG_007955.1:g.11098_11099insGAGAACTTAACTGTGCTTACCTACAGAAAGACAGCACGGGATTTATGCTATCAACTGAGTTTTGTCATCTCCCGAATGACAGCTTCCTGCTGACGATAAAAGCTCTTTTCATCCACTTCAGTGACGGGTA

Transcript Alleles

HGVS Amino-acid change
ENST00000369887.4:c.1243+72_1243+73insGAGAACTTAACTGTGCTTACCTACAGAAAGACAGCACGGGATTTATGCTATCAACTGAGTTTTGTCATCTCCCGAATGACAGCTTCCTGCTGACGATAAAAGCTCTTTTCATCCACTTCAGTGACGGGTA (CYP17A1) MANE Select ENSP00000358903.3:n.1243+72_1243+73insGAG...
ENST00000638190.1:c.940+72_940+73insGAGAACTTAACTGTGCTTACCTACAGAAAGACAGCACGGGATTTATGCTATCAACTGAGTTTTGTCATCTCCCGAATGACAGCTTCCTGCTGACGATAAAAGCTCTTTTCATCCACTTCAGTGACGGGTA (CYP17A1) ENSP00000492539.1:n.940+72_940+73insGAGAA...
ENST00000638272.1:c.787+72_787+73insGAGAACTTAACTGTGCTTACCTACAGAAAGACAGCACGGGATTTATGCTATCAACTGAGTTTTGTCATCTCCCGAATGACAGCTTCCTGCTGACGATAAAAGCTCTTTTCATCCACTTCAGTGACGGGTA (CYP17A1) ENSP00000491508.1:n.787+72_787+73insGAGAA...
ENST00000638971.1:c.1156+72_1156+73insGAGAACTTAACTGTGCTTACCTACAGAAAGACAGCACGGGATTTATGCTATCAACTGAGTTTTGTCATCTCCCGAATGACAGCTTCCTGCTGACGATAAAAGCTCTTTTCATCCACTTCAGTGACGGGTA (CYP17A1) ENSP00000492313.1:n.1156+72_1156+73insGAG...
ENST00000639393.1:c.1246+72_1246+73insGAGAACTTAACTGTGCTTACCTACAGAAAGACAGCACGGGATTTATGCTATCAACTGAGTTTTGTCATCTCCCGAATGACAGCTTCCTGCTGACGATAAAAGCTCTTTTCATCCACTTCAGTGACGGGTA (CYP17A1) ENSP00000492651.1:n.1246+72_1246+73insGAG...
ENST00000640633.1:n.1005+72_1005+73insGAGAACTTAACTGTGCTTACCTACAGAAAGACAGCACGGGATTTATGCTATCAACTGAGTTTTGTCATCTCCCGAATGACAGCTTCCTGCTGACGATAAAAGCTCTTTTCATCCACTTCAGTGACGGGTA (CYP17A1)
ENST00000647664.1:c.*629-163_*629-162insTACCCGTCACTGAAGTGGATGAAAAGAGCTTTTATCGTCAGCAGGAAGCTGTCATTCGGGAGATGACAAAACTCAGTTGATAGCATAAATCCCGTGCTGTCTTTCTGTAGGTAAGCACAGTTAAGTTCTC (WBP1L) ENSP00000498131.1:n.*629-163_*629-162insT...
ENST00000369887.3:c.1243+72_1243+73insGAGAACTTAACTGTGCTTACCTACAGAAAGACAGCACGGGATTTATGCTATCAACTGAGTTTTGTCATCTCCCGAATGACAGCTTCCTGCTGACGATAAAAGCTCTTTTCATCCACTTCAGTGACGGGTA (CYP17A1) ENSP00000358903.3:n.1243+72_1243+73insGAG...
ENST00000469683.1:n.196+72_196+73insGAGAACTTAACTGTGCTTACCTACAGAAAGACAGCACGGGATTTATGCTATCAACTGAGTTTTGTCATCTCCCGAATGACAGCTTCCTGCTGACGATAAAAGCTCTTTTCATCCACTTCAGTGACGGGTA (CYP17A1)
NM_000102.3:c.1243+72_1243+73insGAGAACTTAACTGTGCTTACCTACAGAAAGACAGCACGGGATTTATGCTATCAACTGAGTTTTGTCATCTCCCGAATGACAGCTTCCTGCTGACGATAAAAGCTCTTTTCATCCACTTCAGTGACGGGTA (CYP17A1) NP_000093.1:n.1243+72_1243+73insGAGAACTTA...
NM_000102.4:c.1243+72_1243+73insGAGAACTTAACTGTGCTTACCTACAGAAAGACAGCACGGGATTTATGCTATCAACTGAGTTTTGTCATCTCCCGAATGACAGCTTCCTGCTGACGATAAAAGCTCTTTTCATCCACTTCAGTGACGGGTA (CYP17A1) MANE Select NP_000093.1:n.1243+72_1243+73insGAGAACTTA...