Canonical Allele Identifier: CA368158483
Gene: CYP51A1 HGNC NCBI
AKAP9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92099731A>T , CM000669.2:g.92099731A>T GRCh38
NC_000007.13:g.91729045A>T , CM000669.1:g.91729045A>T GRCh37
NC_000007.12:g.91566981A>T NCBI36
NG_011623.1:g.163857A>T , LRG_331:g.163857A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000691309.1:c.1352-14129T>A (CYP51A1) ENSP00000510368.1:n.1352-14129T>A
ENST00000356239.8:c.10758A>T (AKAP9) MANE Select ENSP00000348573.3:p.Glu3586Asp
ENST00000359028.7:c.10830A>T (AKAP9) ENSP00000351922.4:p.Glu3610Asp
ENST00000394534.7:c.3750A>T (AKAP9) ENSP00000378042.3:p.Glu1250Asp
ENST00000463118.2:n.106A>T (AKAP9)
ENST00000486313.2:c.246A>T (AKAP9) ENSP00000505389.1:p.Glu82Asp
ENST00000487692.2:n.2836A>T (AKAP9)
ENST00000491695.2:c.5403A>T (AKAP9) ENSP00000494626.2:p.Glu1801Asp
ENST00000679448.1:c.*1638A>T (AKAP9) ENSP00000505889.1:n.*1638A>T
ENST00000679457.1:c.10734A>T (AKAP9) ENSP00000505450.1:p.Glu3578Asp
ENST00000679474.1:n.10956A>T (AKAP9)
ENST00000679521.1:c.10704A>T (AKAP9) ENSP00000505456.1:p.Glu3568Asp
ENST00000679821.1:c.10500A>T (AKAP9) ENSP00000506040.1:p.Glu3500Asp
ENST00000680047.1:n.12428A>T (AKAP9)
ENST00000680072.1:c.10581A>T (AKAP9) ENSP00000506581.1:p.Glu3527Asp
ENST00000680181.1:c.10665A>T (AKAP9) ENSP00000505548.1:p.Glu3555Asp
ENST00000680365.1:c.4397A>T (AKAP9) ENSP00000506019.1:n.4397A>T
ENST00000680513.1:c.10617A>T (AKAP9) ENSP00000505284.1:p.Glu3539Asp
ENST00000680534.1:c.10797A>T (AKAP9) ENSP00000506674.1:p.Glu3599Asp
ENST00000680766.1:c.10734A>T (AKAP9) ENSP00000505204.1:p.Glu3578Asp
ENST00000680952.1:c.10734A>T (AKAP9) ENSP00000506407.1:p.Glu3578Asp
ENST00000681216.1:c.4518A>T (AKAP9) ENSP00000505551.1:n.4518A>T
ENST00000681412.1:c.10758A>T (AKAP9) ENSP00000506486.1:p.Glu3586Asp
ENST00000681722.1:c.10734A>T (AKAP9) ENSP00000506566.1:p.Glu3578Asp
ENST00000356239.7:c.10758A>T (AKAP9) ENSP00000348573.3:p.Glu3586Asp
ENST00000359028.6:c.10767A>T (AKAP9) ENSP00000351922.3:p.Glu3589Asp
ENST00000394534.6:c.4296A>T (AKAP9) ENSP00000378042.2:p.Glu1432Asp
ENST00000463118.1:n.106A>T (AKAP9)
ENST00000487258.5:n.2508A>T (AKAP9)
ENST00000487692.1:n.558A>T (AKAP9)
NM_005751.4:c.10758A>T , LRG_331t1:c.10758A>T (AKAP9) NP_005742.4:p.Glu3586Asp
NM_147185.2:c.10734A>T (AKAP9) NP_671714.1:p.Glu3578Asp
XM_006715827.1:c.10617A>T (AKAP9) XP_006715890.1:p.Glu3539Asp
XM_011515709.1:c.10905A>T (AKAP9) XP_011514011.1:p.Glu3635Asp
XM_011515710.1:c.10929A>T (AKAP9) XP_011514012.1:p.Glu3643Asp
XM_011515711.1:c.10869A>T (AKAP9) XP_011514013.1:p.Glu3623Asp
XM_011515712.1:c.10866A>T (AKAP9) XP_011514014.1:p.Glu3622Asp
XM_011515713.1:c.10851A>T (AKAP9) XP_011514015.1:p.Glu3617Asp
XM_011515714.1:c.10890A>T (AKAP9) XP_011514016.1:p.Glu3630Asp
XM_011515716.1:c.10809A>T (AKAP9) XP_011514018.1:p.Glu3603Asp
XM_011515717.1:c.10764A>T (AKAP9) XP_011514019.1:p.Glu3588Asp
XM_011515718.1:c.10794A>T (AKAP9) XP_011514020.1:p.Glu3598Asp
XM_011515719.1:c.10770A>T (AKAP9) XP_011514021.1:p.Glu3590Asp
XM_011515721.1:c.5418A>T (AKAP9) XP_011514023.1:p.Glu1806Asp
XM_011515722.1:c.5379A>T (AKAP9) XP_011514024.1:p.Glu1793Asp
XM_017011642.2:c.10893A>T (AKAP9) XP_016867131.1:p.Glu3631Asp
XM_017011643.2:c.10854A>T (AKAP9) XP_016867132.1:p.Glu3618Asp
XM_017011644.2:c.10893A>T (AKAP9) XP_016867133.1:p.Glu3631Asp
XM_017011645.2:c.10839A>T (AKAP9) XP_016867134.1:p.Glu3613Asp
XM_017011646.2:c.10854A>T (AKAP9) XP_016867135.1:p.Glu3618Asp
XM_017011647.2:c.10800A>T (AKAP9) XP_016867136.1:p.Glu3600Asp
XM_017011648.2:c.10797A>T (AKAP9) XP_016867137.1:p.Glu3599Asp
XM_017011649.2:c.10830A>T (AKAP9) XP_016867138.1:p.Glu3610Asp
XM_017011650.2:c.10758A>T (AKAP9) XP_016867139.1:p.Glu3586Asp
XM_017011651.2:c.10752A>T (AKAP9) XP_016867140.1:p.Glu3584Asp
XM_017011652.2:c.10704A>T (AKAP9) XP_016867141.1:p.Glu3568Asp
XM_017011653.2:c.10665A>T (AKAP9) XP_016867142.1:p.Glu3555Asp
XM_017011654.2:c.10617A>T (AKAP9) XP_016867143.1:p.Glu3539Asp
XM_017011655.2:c.10521A>T (AKAP9) XP_016867144.1:p.Glu3507Asp
XM_017011656.2:c.10521A>T (AKAP9) XP_016867145.1:p.Glu3507Asp
XM_017011657.2:c.6558A>T (AKAP9) XP_016867146.1:p.Glu2186Asp
XM_017011658.2:c.5442A>T (AKAP9) XP_016867147.1:p.Glu1814Asp
XM_017011659.2:c.5403A>T (AKAP9) XP_016867148.1:p.Glu1801Asp
XM_017011660.2:c.5403A>T (AKAP9) XP_016867149.1:p.Glu1801Asp
XM_024446631.1:c.10656A>T (AKAP9) XP_024302399.1:p.Glu3552Asp
NM_147185.3:c.10734A>T (AKAP9) NP_671714.1:p.Glu3578Asp
NM_001379277.1:c.5403A>T (AKAP9) NP_001366206.1:p.Glu1801Asp
NM_005751.5:c.10758A>T (AKAP9) MANE Select NP_005742.4:p.Glu3586Asp