Canonical Allele Identifier: CA456454114
Gene: CYP51A1 HGNC NCBI
AKAP9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.91729036A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92099722A>C , CM000669.2:g.92099722A>C GRCh38
NC_000007.13:g.91729036A>C , CM000669.1:g.91729036A>C GRCh37
NC_000007.12:g.91566972A>C NCBI36
NG_011623.1:g.163848A>C , LRG_331:g.163848A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000691309.1:c.1352-14120T>G (CYP51A1) ENSP00000510368.1:n.1352-14120T>G
ENST00000356239.8:c.10749A>C (AKAP9) MANE Select ENSP00000348573.3:p.Ser3583=
ENST00000359028.7:c.10821A>C (AKAP9) ENSP00000351922.4:p.Ser3607=
ENST00000394534.7:c.3741A>C (AKAP9) ENSP00000378042.3:p.Ser1247=
ENST00000463118.2:n.97A>C (AKAP9)
ENST00000486313.2:c.237A>C (AKAP9) ENSP00000505389.1:p.Ser79=
ENST00000487692.2:n.2827A>C (AKAP9)
ENST00000491695.2:c.5394A>C (AKAP9) ENSP00000494626.2:p.Ser1798=
ENST00000679448.1:c.*1629A>C (AKAP9) ENSP00000505889.1:n.*1629A>C
ENST00000679457.1:c.10725A>C (AKAP9) ENSP00000505450.1:p.Ser3575=
ENST00000679474.1:n.10947A>C (AKAP9)
ENST00000679521.1:c.10695A>C (AKAP9) ENSP00000505456.1:p.Ser3565=
ENST00000679821.1:c.10491A>C (AKAP9) ENSP00000506040.1:p.Ser3497=
ENST00000680047.1:n.12419A>C (AKAP9)
ENST00000680072.1:c.10572A>C (AKAP9) ENSP00000506581.1:p.Ser3524=
ENST00000680181.1:c.10656A>C (AKAP9) ENSP00000505548.1:p.Ser3552=
ENST00000680365.1:c.4388A>C (AKAP9) ENSP00000506019.1:n.4388A>C
ENST00000680513.1:c.10608A>C (AKAP9) ENSP00000505284.1:p.Ser3536=
ENST00000680534.1:c.10788A>C (AKAP9) ENSP00000506674.1:p.Ser3596=
ENST00000680766.1:c.10725A>C (AKAP9) ENSP00000505204.1:p.Ser3575=
ENST00000680952.1:c.10725A>C (AKAP9) ENSP00000506407.1:p.Ser3575=
ENST00000681216.1:c.4509A>C (AKAP9) ENSP00000505551.1:n.4509A>C
ENST00000681412.1:c.10749A>C (AKAP9) ENSP00000506486.1:p.Ser3583=
ENST00000681722.1:c.10725A>C (AKAP9) ENSP00000506566.1:p.Ser3575=
ENST00000356239.7:c.10749A>C (AKAP9) ENSP00000348573.3:p.Ser3583=
ENST00000359028.6:c.10758A>C (AKAP9) ENSP00000351922.3:p.Ser3586=
ENST00000394534.6:c.4287A>C (AKAP9) ENSP00000378042.2:p.Ser1429=
ENST00000463118.1:n.97A>C (AKAP9)
ENST00000487258.5:n.2499A>C (AKAP9)
ENST00000487692.1:n.549A>C (AKAP9)
NM_005751.4:c.10749A>C , LRG_331t1:c.10749A>C (AKAP9) NP_005742.4:p.Ser3583=
NM_147185.2:c.10725A>C (AKAP9) NP_671714.1:p.Ser3575=
XM_006715827.1:c.10608A>C (AKAP9) XP_006715890.1:p.Ser3536=
XM_011515709.1:c.10896A>C (AKAP9) XP_011514011.1:p.Ser3632=
XM_011515710.1:c.10920A>C (AKAP9) XP_011514012.1:p.Ser3640=
XM_011515711.1:c.10860A>C (AKAP9) XP_011514013.1:p.Ser3620=
XM_011515712.1:c.10857A>C (AKAP9) XP_011514014.1:p.Ser3619=
XM_011515713.1:c.10842A>C (AKAP9) XP_011514015.1:p.Ser3614=
XM_011515714.1:c.10881A>C (AKAP9) XP_011514016.1:p.Ser3627=
XM_011515716.1:c.10800A>C (AKAP9) XP_011514018.1:p.Ser3600=
XM_011515717.1:c.10755A>C (AKAP9) XP_011514019.1:p.Ser3585=
XM_011515718.1:c.10785A>C (AKAP9) XP_011514020.1:p.Ser3595=
XM_011515719.1:c.10761A>C (AKAP9) XP_011514021.1:p.Ser3587=
XM_011515721.1:c.5409A>C (AKAP9) XP_011514023.1:p.Ser1803=
XM_011515722.1:c.5370A>C (AKAP9) XP_011514024.1:p.Ser1790=
XM_017011642.2:c.10884A>C (AKAP9) XP_016867131.1:p.Ser3628=
XM_017011643.2:c.10845A>C (AKAP9) XP_016867132.1:p.Ser3615=
XM_017011644.2:c.10884A>C (AKAP9) XP_016867133.1:p.Ser3628=
XM_017011645.2:c.10830A>C (AKAP9) XP_016867134.1:p.Ser3610=
XM_017011646.2:c.10845A>C (AKAP9) XP_016867135.1:p.Ser3615=
XM_017011647.2:c.10791A>C (AKAP9) XP_016867136.1:p.Ser3597=
XM_017011648.2:c.10788A>C (AKAP9) XP_016867137.1:p.Ser3596=
XM_017011649.2:c.10821A>C (AKAP9) XP_016867138.1:p.Ser3607=
XM_017011650.2:c.10749A>C (AKAP9) XP_016867139.1:p.Ser3583=
XM_017011651.2:c.10743A>C (AKAP9) XP_016867140.1:p.Ser3581=
XM_017011652.2:c.10695A>C (AKAP9) XP_016867141.1:p.Ser3565=
XM_017011653.2:c.10656A>C (AKAP9) XP_016867142.1:p.Ser3552=
XM_017011654.2:c.10608A>C (AKAP9) XP_016867143.1:p.Ser3536=
XM_017011655.2:c.10512A>C (AKAP9) XP_016867144.1:p.Ser3504=
XM_017011656.2:c.10512A>C (AKAP9) XP_016867145.1:p.Ser3504=
XM_017011657.2:c.6549A>C (AKAP9) XP_016867146.1:p.Ser2183=
XM_017011658.2:c.5433A>C (AKAP9) XP_016867147.1:p.Ser1811=
XM_017011659.2:c.5394A>C (AKAP9) XP_016867148.1:p.Ser1798=
XM_017011660.2:c.5394A>C (AKAP9) XP_016867149.1:p.Ser1798=
XM_024446631.1:c.10647A>C (AKAP9) XP_024302399.1:p.Ser3549=
NM_147185.3:c.10725A>C (AKAP9) NP_671714.1:p.Ser3575=
NM_001379277.1:c.5394A>C (AKAP9) NP_001366206.1:p.Ser1798=
NM_005751.5:c.10749A>C (AKAP9) MANE Select NP_005742.4:p.Ser3583=