Canonical Allele Identifier: CA368158479
Gene: CYP51A1 HGNC NCBI
AKAP9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92099730A>T , CM000669.2:g.92099730A>T GRCh38
NC_000007.13:g.91729044A>T , CM000669.1:g.91729044A>T GRCh37
NC_000007.12:g.91566980A>T NCBI36
NG_011623.1:g.163856A>T , LRG_331:g.163856A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000691309.1:c.1352-14128T>A (CYP51A1) ENSP00000510368.1:n.1352-14128T>A
ENST00000356239.8:c.10757A>T (AKAP9) MANE Select ENSP00000348573.3:p.Glu3586Val
ENST00000359028.7:c.10829A>T (AKAP9) ENSP00000351922.4:p.Glu3610Val
ENST00000394534.7:c.3749A>T (AKAP9) ENSP00000378042.3:p.Glu1250Val
ENST00000463118.2:n.105A>T (AKAP9)
ENST00000486313.2:c.245A>T (AKAP9) ENSP00000505389.1:p.Glu82Val
ENST00000487692.2:n.2835A>T (AKAP9)
ENST00000491695.2:c.5402A>T (AKAP9) ENSP00000494626.2:p.Glu1801Val
ENST00000679448.1:c.*1637A>T (AKAP9) ENSP00000505889.1:n.*1637A>T
ENST00000679457.1:c.10733A>T (AKAP9) ENSP00000505450.1:p.Glu3578Val
ENST00000679474.1:n.10955A>T (AKAP9)
ENST00000679521.1:c.10703A>T (AKAP9) ENSP00000505456.1:p.Glu3568Val
ENST00000679821.1:c.10499A>T (AKAP9) ENSP00000506040.1:p.Glu3500Val
ENST00000680047.1:n.12427A>T (AKAP9)
ENST00000680072.1:c.10580A>T (AKAP9) ENSP00000506581.1:p.Glu3527Val
ENST00000680181.1:c.10664A>T (AKAP9) ENSP00000505548.1:p.Glu3555Val
ENST00000680365.1:c.4396A>T (AKAP9) ENSP00000506019.1:n.4396A>T
ENST00000680513.1:c.10616A>T (AKAP9) ENSP00000505284.1:p.Glu3539Val
ENST00000680534.1:c.10796A>T (AKAP9) ENSP00000506674.1:p.Glu3599Val
ENST00000680766.1:c.10733A>T (AKAP9) ENSP00000505204.1:p.Glu3578Val
ENST00000680952.1:c.10733A>T (AKAP9) ENSP00000506407.1:p.Glu3578Val
ENST00000681216.1:c.4517A>T (AKAP9) ENSP00000505551.1:n.4517A>T
ENST00000681412.1:c.10757A>T (AKAP9) ENSP00000506486.1:p.Glu3586Val
ENST00000681722.1:c.10733A>T (AKAP9) ENSP00000506566.1:p.Glu3578Val
ENST00000356239.7:c.10757A>T (AKAP9) ENSP00000348573.3:p.Glu3586Val
ENST00000359028.6:c.10766A>T (AKAP9) ENSP00000351922.3:p.Glu3589Val
ENST00000394534.6:c.4295A>T (AKAP9) ENSP00000378042.2:p.Glu1432Val
ENST00000463118.1:n.105A>T (AKAP9)
ENST00000487258.5:n.2507A>T (AKAP9)
ENST00000487692.1:n.557A>T (AKAP9)
NM_005751.4:c.10757A>T , LRG_331t1:c.10757A>T (AKAP9) NP_005742.4:p.Glu3586Val
NM_147185.2:c.10733A>T (AKAP9) NP_671714.1:p.Glu3578Val
XM_006715827.1:c.10616A>T (AKAP9) XP_006715890.1:p.Glu3539Val
XM_011515709.1:c.10904A>T (AKAP9) XP_011514011.1:p.Glu3635Val
XM_011515710.1:c.10928A>T (AKAP9) XP_011514012.1:p.Glu3643Val
XM_011515711.1:c.10868A>T (AKAP9) XP_011514013.1:p.Glu3623Val
XM_011515712.1:c.10865A>T (AKAP9) XP_011514014.1:p.Glu3622Val
XM_011515713.1:c.10850A>T (AKAP9) XP_011514015.1:p.Glu3617Val
XM_011515714.1:c.10889A>T (AKAP9) XP_011514016.1:p.Glu3630Val
XM_011515716.1:c.10808A>T (AKAP9) XP_011514018.1:p.Glu3603Val
XM_011515717.1:c.10763A>T (AKAP9) XP_011514019.1:p.Glu3588Val
XM_011515718.1:c.10793A>T (AKAP9) XP_011514020.1:p.Glu3598Val
XM_011515719.1:c.10769A>T (AKAP9) XP_011514021.1:p.Glu3590Val
XM_011515721.1:c.5417A>T (AKAP9) XP_011514023.1:p.Glu1806Val
XM_011515722.1:c.5378A>T (AKAP9) XP_011514024.1:p.Glu1793Val
XM_017011642.2:c.10892A>T (AKAP9) XP_016867131.1:p.Glu3631Val
XM_017011643.2:c.10853A>T (AKAP9) XP_016867132.1:p.Glu3618Val
XM_017011644.2:c.10892A>T (AKAP9) XP_016867133.1:p.Glu3631Val
XM_017011645.2:c.10838A>T (AKAP9) XP_016867134.1:p.Glu3613Val
XM_017011646.2:c.10853A>T (AKAP9) XP_016867135.1:p.Glu3618Val
XM_017011647.2:c.10799A>T (AKAP9) XP_016867136.1:p.Glu3600Val
XM_017011648.2:c.10796A>T (AKAP9) XP_016867137.1:p.Glu3599Val
XM_017011649.2:c.10829A>T (AKAP9) XP_016867138.1:p.Glu3610Val
XM_017011650.2:c.10757A>T (AKAP9) XP_016867139.1:p.Glu3586Val
XM_017011651.2:c.10751A>T (AKAP9) XP_016867140.1:p.Glu3584Val
XM_017011652.2:c.10703A>T (AKAP9) XP_016867141.1:p.Glu3568Val
XM_017011653.2:c.10664A>T (AKAP9) XP_016867142.1:p.Glu3555Val
XM_017011654.2:c.10616A>T (AKAP9) XP_016867143.1:p.Glu3539Val
XM_017011655.2:c.10520A>T (AKAP9) XP_016867144.1:p.Glu3507Val
XM_017011656.2:c.10520A>T (AKAP9) XP_016867145.1:p.Glu3507Val
XM_017011657.2:c.6557A>T (AKAP9) XP_016867146.1:p.Glu2186Val
XM_017011658.2:c.5441A>T (AKAP9) XP_016867147.1:p.Glu1814Val
XM_017011659.2:c.5402A>T (AKAP9) XP_016867148.1:p.Glu1801Val
XM_017011660.2:c.5402A>T (AKAP9) XP_016867149.1:p.Glu1801Val
XM_024446631.1:c.10655A>T (AKAP9) XP_024302399.1:p.Glu3552Val
NM_147185.3:c.10733A>T (AKAP9) NP_671714.1:p.Glu3578Val
NM_001379277.1:c.5402A>T (AKAP9) NP_001366206.1:p.Glu1801Val
NM_005751.5:c.10757A>T (AKAP9) MANE Select NP_005742.4:p.Glu3586Val