Canonical Allele Identifier: CA368158917
Gene: CYP51A1 HGNC NCBI
AKAP9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92099825G>T , CM000669.2:g.92099825G>T GRCh38
NC_000007.13:g.91729139G>T , CM000669.1:g.91729139G>T GRCh37
NC_000007.12:g.91567075G>T NCBI36
NG_011623.1:g.163951G>T , LRG_331:g.163951G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000691309.1:c.1352-14223C>A (CYP51A1) ENSP00000510368.1:n.1352-14223C>A
ENST00000356239.8:c.10852G>T (AKAP9) MANE Select ENSP00000348573.3:p.Glu3618Ter
ENST00000359028.7:c.10924G>T (AKAP9) ENSP00000351922.4:p.Glu3642Ter
ENST00000394534.7:c.3844G>T (AKAP9) ENSP00000378042.3:p.Glu1282Ter
ENST00000463118.2:n.200G>T (AKAP9)
ENST00000486313.2:c.340G>T (AKAP9) ENSP00000505389.1:p.Glu114Ter
ENST00000487692.2:n.2930G>T (AKAP9)
ENST00000491695.2:c.5497G>T (AKAP9) ENSP00000494626.2:p.Glu1833Ter
ENST00000679448.1:c.*1732G>T (AKAP9) ENSP00000505889.1:n.*1732G>T
ENST00000679457.1:c.10828G>T (AKAP9) ENSP00000505450.1:p.Glu3610Ter
ENST00000679474.1:n.11050G>T (AKAP9)
ENST00000679521.1:c.10798G>T (AKAP9) ENSP00000505456.1:p.Glu3600Ter
ENST00000679821.1:c.10594G>T (AKAP9) ENSP00000506040.1:p.Glu3532Ter
ENST00000680047.1:n.12522G>T (AKAP9)
ENST00000680072.1:c.10675G>T (AKAP9) ENSP00000506581.1:p.Glu3559Ter
ENST00000680181.1:c.10759G>T (AKAP9) ENSP00000505548.1:p.Glu3587Ter
ENST00000680365.1:c.4491G>T (AKAP9) ENSP00000506019.1:n.4491G>T
ENST00000680513.1:c.10711G>T (AKAP9) ENSP00000505284.1:p.Glu3571Ter
ENST00000680534.1:c.10891G>T (AKAP9) ENSP00000506674.1:p.Glu3631Ter
ENST00000680766.1:c.10828G>T (AKAP9) ENSP00000505204.1:p.Glu3610Ter
ENST00000680952.1:c.10828G>T (AKAP9) ENSP00000506407.1:p.Glu3610Ter
ENST00000681216.1:c.4612G>T (AKAP9) ENSP00000505551.1:n.4612G>T
ENST00000681412.1:c.10852G>T (AKAP9) ENSP00000506486.1:p.Glu3618Ter
ENST00000681722.1:c.10828G>T (AKAP9) ENSP00000506566.1:p.Glu3610Ter
ENST00000356239.7:c.10852G>T (AKAP9) ENSP00000348573.3:p.Glu3618Ter
ENST00000359028.6:c.10861G>T (AKAP9) ENSP00000351922.3:p.Glu3621Ter
ENST00000394534.6:c.4390G>T (AKAP9) ENSP00000378042.2:p.Glu1464Ter
ENST00000463118.1:n.200G>T (AKAP9)
ENST00000487258.5:n.2602G>T (AKAP9)
ENST00000487692.1:n.652G>T (AKAP9)
NM_005751.4:c.10852G>T , LRG_331t1:c.10852G>T (AKAP9) NP_005742.4:p.Glu3618Ter
NM_147185.2:c.10828G>T (AKAP9) NP_671714.1:p.Glu3610Ter
XM_006715827.1:c.10711G>T (AKAP9) XP_006715890.1:p.Glu3571Ter
XM_011515709.1:c.10999G>T (AKAP9) XP_011514011.1:p.Glu3667Ter
XM_011515710.1:c.11023G>T (AKAP9) XP_011514012.1:p.Glu3675Ter
XM_011515711.1:c.10963G>T (AKAP9) XP_011514013.1:p.Glu3655Ter
XM_011515712.1:c.10960G>T (AKAP9) XP_011514014.1:p.Glu3654Ter
XM_011515713.1:c.10945G>T (AKAP9) XP_011514015.1:p.Glu3649Ter
XM_011515714.1:c.10984G>T (AKAP9) XP_011514016.1:p.Glu3662Ter
XM_011515716.1:c.10903G>T (AKAP9) XP_011514018.1:p.Glu3635Ter
XM_011515717.1:c.10858G>T (AKAP9) XP_011514019.1:p.Glu3620Ter
XM_011515718.1:c.10888G>T (AKAP9) XP_011514020.1:p.Glu3630Ter
XM_011515719.1:c.10864G>T (AKAP9) XP_011514021.1:p.Glu3622Ter
XM_011515721.1:c.5512G>T (AKAP9) XP_011514023.1:p.Glu1838Ter
XM_011515722.1:c.5473G>T (AKAP9) XP_011514024.1:p.Glu1825Ter
XM_017011642.2:c.10987G>T (AKAP9) XP_016867131.1:p.Glu3663Ter
XM_017011643.2:c.10948G>T (AKAP9) XP_016867132.1:p.Glu3650Ter
XM_017011644.2:c.10987G>T (AKAP9) XP_016867133.1:p.Glu3663Ter
XM_017011645.2:c.10933G>T (AKAP9) XP_016867134.1:p.Glu3645Ter
XM_017011646.2:c.10948G>T (AKAP9) XP_016867135.1:p.Glu3650Ter
XM_017011647.2:c.10894G>T (AKAP9) XP_016867136.1:p.Glu3632Ter
XM_017011648.2:c.10891G>T (AKAP9) XP_016867137.1:p.Glu3631Ter
XM_017011649.2:c.10924G>T (AKAP9) XP_016867138.1:p.Glu3642Ter
XM_017011650.2:c.10852G>T (AKAP9) XP_016867139.1:p.Glu3618Ter
XM_017011651.2:c.10846G>T (AKAP9) XP_016867140.1:p.Glu3616Ter
XM_017011652.2:c.10798G>T (AKAP9) XP_016867141.1:p.Glu3600Ter
XM_017011653.2:c.10759G>T (AKAP9) XP_016867142.1:p.Glu3587Ter
XM_017011654.2:c.10711G>T (AKAP9) XP_016867143.1:p.Glu3571Ter
XM_017011655.2:c.10615G>T (AKAP9) XP_016867144.1:p.Glu3539Ter
XM_017011656.2:c.10615G>T (AKAP9) XP_016867145.1:p.Glu3539Ter
XM_017011657.2:c.6652G>T (AKAP9) XP_016867146.1:p.Glu2218Ter
XM_017011658.2:c.5536G>T (AKAP9) XP_016867147.1:p.Glu1846Ter
XM_017011659.2:c.5497G>T (AKAP9) XP_016867148.1:p.Glu1833Ter
XM_017011660.2:c.5497G>T (AKAP9) XP_016867149.1:p.Glu1833Ter
XM_024446631.1:c.10750G>T (AKAP9) XP_024302399.1:p.Glu3584Ter
NM_147185.3:c.10828G>T (AKAP9) NP_671714.1:p.Glu3610Ter
NM_001379277.1:c.5497G>T (AKAP9) NP_001366206.1:p.Glu1833Ter
NM_005751.5:c.10852G>T (AKAP9) MANE Select NP_005742.4:p.Glu3618Ter