Canonical Allele Identifier: CA368158417
Gene: CYP51A1 HGNC NCBI
AKAP9 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000691309.1:c.1352-14118A>C (CYP51A1) ENSP00000510368.1:n.1352-14118A>C
ENST00000356239.8:c.10747T>G (AKAP9) MANE Select ENSP00000348573.3:p.Ser3583Ala
ENST00000359028.7:c.10819T>G (AKAP9) ENSP00000351922.4:p.Ser3607Ala
ENST00000394534.7:c.3739T>G (AKAP9) ENSP00000378042.3:p.Ser1247Ala
ENST00000463118.2:n.95T>G (AKAP9)
ENST00000486313.2:c.235T>G (AKAP9) ENSP00000505389.1:p.Ser79Ala
ENST00000487692.2:n.2825T>G (AKAP9)
ENST00000491695.2:c.5392T>G (AKAP9) ENSP00000494626.2:p.Ser1798Ala
ENST00000679448.1:c.*1627T>G (AKAP9) ENSP00000505889.1:n.*1627T>G
ENST00000679457.1:c.10723T>G (AKAP9) ENSP00000505450.1:p.Ser3575Ala
ENST00000679474.1:n.10945T>G (AKAP9)
ENST00000679521.1:c.10693T>G (AKAP9) ENSP00000505456.1:p.Ser3565Ala
ENST00000679821.1:c.10489T>G (AKAP9) ENSP00000506040.1:p.Ser3497Ala
ENST00000680047.1:n.12417T>G (AKAP9)
ENST00000680072.1:c.10570T>G (AKAP9) ENSP00000506581.1:p.Ser3524Ala
ENST00000680181.1:c.10654T>G (AKAP9) ENSP00000505548.1:p.Ser3552Ala
ENST00000680365.1:c.4386T>G (AKAP9) ENSP00000506019.1:n.4386T>G
ENST00000680513.1:c.10606T>G (AKAP9) ENSP00000505284.1:p.Ser3536Ala
ENST00000680534.1:c.10786T>G (AKAP9) ENSP00000506674.1:p.Ser3596Ala
ENST00000680766.1:c.10723T>G (AKAP9) ENSP00000505204.1:p.Ser3575Ala
ENST00000680952.1:c.10723T>G (AKAP9) ENSP00000506407.1:p.Ser3575Ala
ENST00000681216.1:c.4507T>G (AKAP9) ENSP00000505551.1:n.4507T>G
ENST00000681412.1:c.10747T>G (AKAP9) ENSP00000506486.1:p.Ser3583Ala
ENST00000681722.1:c.10723T>G (AKAP9) ENSP00000506566.1:p.Ser3575Ala
ENST00000356239.7:c.10747T>G (AKAP9) ENSP00000348573.3:p.Ser3583Ala
ENST00000359028.6:c.10756T>G (AKAP9) ENSP00000351922.3:p.Ser3586Ala
ENST00000394534.6:c.4285T>G (AKAP9) ENSP00000378042.2:p.Ser1429Ala
ENST00000463118.1:n.95T>G (AKAP9)
ENST00000487258.5:n.2497T>G (AKAP9)
ENST00000487692.1:n.547T>G (AKAP9)
NM_005751.4:c.10747T>G , LRG_331t1:c.10747T>G (AKAP9) NP_005742.4:p.Ser3583Ala
NM_147185.2:c.10723T>G (AKAP9) NP_671714.1:p.Ser3575Ala
XM_006715827.1:c.10606T>G (AKAP9) XP_006715890.1:p.Ser3536Ala
XM_011515709.1:c.10894T>G (AKAP9) XP_011514011.1:p.Ser3632Ala
XM_011515710.1:c.10918T>G (AKAP9) XP_011514012.1:p.Ser3640Ala
XM_011515711.1:c.10858T>G (AKAP9) XP_011514013.1:p.Ser3620Ala
XM_011515712.1:c.10855T>G (AKAP9) XP_011514014.1:p.Ser3619Ala
XM_011515713.1:c.10840T>G (AKAP9) XP_011514015.1:p.Ser3614Ala
XM_011515714.1:c.10879T>G (AKAP9) XP_011514016.1:p.Ser3627Ala
XM_011515716.1:c.10798T>G (AKAP9) XP_011514018.1:p.Ser3600Ala
XM_011515717.1:c.10753T>G (AKAP9) XP_011514019.1:p.Ser3585Ala
XM_011515718.1:c.10783T>G (AKAP9) XP_011514020.1:p.Ser3595Ala
XM_011515719.1:c.10759T>G (AKAP9) XP_011514021.1:p.Ser3587Ala
XM_011515721.1:c.5407T>G (AKAP9) XP_011514023.1:p.Ser1803Ala
XM_011515722.1:c.5368T>G (AKAP9) XP_011514024.1:p.Ser1790Ala
XM_017011642.2:c.10882T>G (AKAP9) XP_016867131.1:p.Ser3628Ala
XM_017011643.2:c.10843T>G (AKAP9) XP_016867132.1:p.Ser3615Ala
XM_017011644.2:c.10882T>G (AKAP9) XP_016867133.1:p.Ser3628Ala
XM_017011645.2:c.10828T>G (AKAP9) XP_016867134.1:p.Ser3610Ala
XM_017011646.2:c.10843T>G (AKAP9) XP_016867135.1:p.Ser3615Ala
XM_017011647.2:c.10789T>G (AKAP9) XP_016867136.1:p.Ser3597Ala
XM_017011648.2:c.10786T>G (AKAP9) XP_016867137.1:p.Ser3596Ala
XM_017011649.2:c.10819T>G (AKAP9) XP_016867138.1:p.Ser3607Ala
XM_017011650.2:c.10747T>G (AKAP9) XP_016867139.1:p.Ser3583Ala
XM_017011651.2:c.10741T>G (AKAP9) XP_016867140.1:p.Ser3581Ala
XM_017011652.2:c.10693T>G (AKAP9) XP_016867141.1:p.Ser3565Ala
XM_017011653.2:c.10654T>G (AKAP9) XP_016867142.1:p.Ser3552Ala
XM_017011654.2:c.10606T>G (AKAP9) XP_016867143.1:p.Ser3536Ala
XM_017011655.2:c.10510T>G (AKAP9) XP_016867144.1:p.Ser3504Ala
XM_017011656.2:c.10510T>G (AKAP9) XP_016867145.1:p.Ser3504Ala
XM_017011657.2:c.6547T>G (AKAP9) XP_016867146.1:p.Ser2183Ala
XM_017011658.2:c.5431T>G (AKAP9) XP_016867147.1:p.Ser1811Ala
XM_017011659.2:c.5392T>G (AKAP9) XP_016867148.1:p.Ser1798Ala
XM_017011660.2:c.5392T>G (AKAP9) XP_016867149.1:p.Ser1798Ala
XM_024446631.1:c.10645T>G (AKAP9) XP_024302399.1:p.Ser3549Ala
NM_147185.3:c.10723T>G (AKAP9) NP_671714.1:p.Ser3575Ala
NM_001379277.1:c.5392T>G (AKAP9) NP_001366206.1:p.Ser1798Ala
NM_005751.5:c.10747T>G (AKAP9) MANE Select NP_005742.4:p.Ser3583Ala