Canonical Allele Identifier: CA368158413
Gene: CYP51A1 HGNC NCBI
AKAP9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92099720T>A , CM000669.2:g.92099720T>A GRCh38
NC_000007.13:g.91729034T>A , CM000669.1:g.91729034T>A GRCh37
NC_000007.12:g.91566970T>A NCBI36
NG_011623.1:g.163846T>A , LRG_331:g.163846T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000691309.1:c.1352-14118A>T (CYP51A1) ENSP00000510368.1:n.1352-14118A>T
ENST00000356239.8:c.10747T>A (AKAP9) MANE Select ENSP00000348573.3:p.Ser3583Thr
ENST00000359028.7:c.10819T>A (AKAP9) ENSP00000351922.4:p.Ser3607Thr
ENST00000394534.7:c.3739T>A (AKAP9) ENSP00000378042.3:p.Ser1247Thr
ENST00000463118.2:n.95T>A (AKAP9)
ENST00000486313.2:c.235T>A (AKAP9) ENSP00000505389.1:p.Ser79Thr
ENST00000487692.2:n.2825T>A (AKAP9)
ENST00000491695.2:c.5392T>A (AKAP9) ENSP00000494626.2:p.Ser1798Thr
ENST00000679448.1:c.*1627T>A (AKAP9) ENSP00000505889.1:n.*1627T>A
ENST00000679457.1:c.10723T>A (AKAP9) ENSP00000505450.1:p.Ser3575Thr
ENST00000679474.1:n.10945T>A (AKAP9)
ENST00000679521.1:c.10693T>A (AKAP9) ENSP00000505456.1:p.Ser3565Thr
ENST00000679821.1:c.10489T>A (AKAP9) ENSP00000506040.1:p.Ser3497Thr
ENST00000680047.1:n.12417T>A (AKAP9)
ENST00000680072.1:c.10570T>A (AKAP9) ENSP00000506581.1:p.Ser3524Thr
ENST00000680181.1:c.10654T>A (AKAP9) ENSP00000505548.1:p.Ser3552Thr
ENST00000680365.1:c.4386T>A (AKAP9) ENSP00000506019.1:n.4386T>A
ENST00000680513.1:c.10606T>A (AKAP9) ENSP00000505284.1:p.Ser3536Thr
ENST00000680534.1:c.10786T>A (AKAP9) ENSP00000506674.1:p.Ser3596Thr
ENST00000680766.1:c.10723T>A (AKAP9) ENSP00000505204.1:p.Ser3575Thr
ENST00000680952.1:c.10723T>A (AKAP9) ENSP00000506407.1:p.Ser3575Thr
ENST00000681216.1:c.4507T>A (AKAP9) ENSP00000505551.1:n.4507T>A
ENST00000681412.1:c.10747T>A (AKAP9) ENSP00000506486.1:p.Ser3583Thr
ENST00000681722.1:c.10723T>A (AKAP9) ENSP00000506566.1:p.Ser3575Thr
ENST00000356239.7:c.10747T>A (AKAP9) ENSP00000348573.3:p.Ser3583Thr
ENST00000359028.6:c.10756T>A (AKAP9) ENSP00000351922.3:p.Ser3586Thr
ENST00000394534.6:c.4285T>A (AKAP9) ENSP00000378042.2:p.Ser1429Thr
ENST00000463118.1:n.95T>A (AKAP9)
ENST00000487258.5:n.2497T>A (AKAP9)
ENST00000487692.1:n.547T>A (AKAP9)
NM_005751.4:c.10747T>A , LRG_331t1:c.10747T>A (AKAP9) NP_005742.4:p.Ser3583Thr
NM_147185.2:c.10723T>A (AKAP9) NP_671714.1:p.Ser3575Thr
XM_006715827.1:c.10606T>A (AKAP9) XP_006715890.1:p.Ser3536Thr
XM_011515709.1:c.10894T>A (AKAP9) XP_011514011.1:p.Ser3632Thr
XM_011515710.1:c.10918T>A (AKAP9) XP_011514012.1:p.Ser3640Thr
XM_011515711.1:c.10858T>A (AKAP9) XP_011514013.1:p.Ser3620Thr
XM_011515712.1:c.10855T>A (AKAP9) XP_011514014.1:p.Ser3619Thr
XM_011515713.1:c.10840T>A (AKAP9) XP_011514015.1:p.Ser3614Thr
XM_011515714.1:c.10879T>A (AKAP9) XP_011514016.1:p.Ser3627Thr
XM_011515716.1:c.10798T>A (AKAP9) XP_011514018.1:p.Ser3600Thr
XM_011515717.1:c.10753T>A (AKAP9) XP_011514019.1:p.Ser3585Thr
XM_011515718.1:c.10783T>A (AKAP9) XP_011514020.1:p.Ser3595Thr
XM_011515719.1:c.10759T>A (AKAP9) XP_011514021.1:p.Ser3587Thr
XM_011515721.1:c.5407T>A (AKAP9) XP_011514023.1:p.Ser1803Thr
XM_011515722.1:c.5368T>A (AKAP9) XP_011514024.1:p.Ser1790Thr
XM_017011642.2:c.10882T>A (AKAP9) XP_016867131.1:p.Ser3628Thr
XM_017011643.2:c.10843T>A (AKAP9) XP_016867132.1:p.Ser3615Thr
XM_017011644.2:c.10882T>A (AKAP9) XP_016867133.1:p.Ser3628Thr
XM_017011645.2:c.10828T>A (AKAP9) XP_016867134.1:p.Ser3610Thr
XM_017011646.2:c.10843T>A (AKAP9) XP_016867135.1:p.Ser3615Thr
XM_017011647.2:c.10789T>A (AKAP9) XP_016867136.1:p.Ser3597Thr
XM_017011648.2:c.10786T>A (AKAP9) XP_016867137.1:p.Ser3596Thr
XM_017011649.2:c.10819T>A (AKAP9) XP_016867138.1:p.Ser3607Thr
XM_017011650.2:c.10747T>A (AKAP9) XP_016867139.1:p.Ser3583Thr
XM_017011651.2:c.10741T>A (AKAP9) XP_016867140.1:p.Ser3581Thr
XM_017011652.2:c.10693T>A (AKAP9) XP_016867141.1:p.Ser3565Thr
XM_017011653.2:c.10654T>A (AKAP9) XP_016867142.1:p.Ser3552Thr
XM_017011654.2:c.10606T>A (AKAP9) XP_016867143.1:p.Ser3536Thr
XM_017011655.2:c.10510T>A (AKAP9) XP_016867144.1:p.Ser3504Thr
XM_017011656.2:c.10510T>A (AKAP9) XP_016867145.1:p.Ser3504Thr
XM_017011657.2:c.6547T>A (AKAP9) XP_016867146.1:p.Ser2183Thr
XM_017011658.2:c.5431T>A (AKAP9) XP_016867147.1:p.Ser1811Thr
XM_017011659.2:c.5392T>A (AKAP9) XP_016867148.1:p.Ser1798Thr
XM_017011660.2:c.5392T>A (AKAP9) XP_016867149.1:p.Ser1798Thr
XM_024446631.1:c.10645T>A (AKAP9) XP_024302399.1:p.Ser3549Thr
NM_147185.3:c.10723T>A (AKAP9) NP_671714.1:p.Ser3575Thr
NM_001379277.1:c.5392T>A (AKAP9) NP_001366206.1:p.Ser1798Thr
NM_005751.5:c.10747T>A (AKAP9) MANE Select NP_005742.4:p.Ser3583Thr