Canonical Allele Identifier: CA368158915
Gene: CYP51A1 HGNC NCBI
AKAP9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92099824A>T , CM000669.2:g.92099824A>T GRCh38
NC_000007.13:g.91729138A>T , CM000669.1:g.91729138A>T GRCh37
NC_000007.12:g.91567074A>T NCBI36
NG_011623.1:g.163950A>T , LRG_331:g.163950A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000691309.1:c.1352-14222T>A (CYP51A1) ENSP00000510368.1:n.1352-14222T>A
ENST00000356239.8:c.10851A>T (AKAP9) MANE Select ENSP00000348573.3:p.Glu3617Asp
ENST00000359028.7:c.10923A>T (AKAP9) ENSP00000351922.4:p.Glu3641Asp
ENST00000394534.7:c.3843A>T (AKAP9) ENSP00000378042.3:p.Glu1281Asp
ENST00000463118.2:n.199A>T (AKAP9)
ENST00000486313.2:c.339A>T (AKAP9) ENSP00000505389.1:p.Glu113Asp
ENST00000487692.2:n.2929A>T (AKAP9)
ENST00000491695.2:c.5496A>T (AKAP9) ENSP00000494626.2:p.Glu1832Asp
ENST00000679448.1:c.*1731A>T (AKAP9) ENSP00000505889.1:n.*1731A>T
ENST00000679457.1:c.10827A>T (AKAP9) ENSP00000505450.1:p.Glu3609Asp
ENST00000679474.1:n.11049A>T (AKAP9)
ENST00000679521.1:c.10797A>T (AKAP9) ENSP00000505456.1:p.Glu3599Asp
ENST00000679821.1:c.10593A>T (AKAP9) ENSP00000506040.1:p.Glu3531Asp
ENST00000680047.1:n.12521A>T (AKAP9)
ENST00000680072.1:c.10674A>T (AKAP9) ENSP00000506581.1:p.Glu3558Asp
ENST00000680181.1:c.10758A>T (AKAP9) ENSP00000505548.1:p.Glu3586Asp
ENST00000680365.1:c.4490A>T (AKAP9) ENSP00000506019.1:n.4490A>T
ENST00000680513.1:c.10710A>T (AKAP9) ENSP00000505284.1:p.Glu3570Asp
ENST00000680534.1:c.10890A>T (AKAP9) ENSP00000506674.1:p.Glu3630Asp
ENST00000680766.1:c.10827A>T (AKAP9) ENSP00000505204.1:p.Glu3609Asp
ENST00000680952.1:c.10827A>T (AKAP9) ENSP00000506407.1:p.Glu3609Asp
ENST00000681216.1:c.4611A>T (AKAP9) ENSP00000505551.1:n.4611A>T
ENST00000681412.1:c.10851A>T (AKAP9) ENSP00000506486.1:p.Glu3617Asp
ENST00000681722.1:c.10827A>T (AKAP9) ENSP00000506566.1:p.Glu3609Asp
ENST00000356239.7:c.10851A>T (AKAP9) ENSP00000348573.3:p.Glu3617Asp
ENST00000359028.6:c.10860A>T (AKAP9) ENSP00000351922.3:p.Glu3620Asp
ENST00000394534.6:c.4389A>T (AKAP9) ENSP00000378042.2:p.Glu1463Asp
ENST00000463118.1:n.199A>T (AKAP9)
ENST00000487258.5:n.2601A>T (AKAP9)
ENST00000487692.1:n.651A>T (AKAP9)
NM_005751.4:c.10851A>T , LRG_331t1:c.10851A>T (AKAP9) NP_005742.4:p.Glu3617Asp
NM_147185.2:c.10827A>T (AKAP9) NP_671714.1:p.Glu3609Asp
XM_006715827.1:c.10710A>T (AKAP9) XP_006715890.1:p.Glu3570Asp
XM_011515709.1:c.10998A>T (AKAP9) XP_011514011.1:p.Glu3666Asp
XM_011515710.1:c.11022A>T (AKAP9) XP_011514012.1:p.Glu3674Asp
XM_011515711.1:c.10962A>T (AKAP9) XP_011514013.1:p.Glu3654Asp
XM_011515712.1:c.10959A>T (AKAP9) XP_011514014.1:p.Glu3653Asp
XM_011515713.1:c.10944A>T (AKAP9) XP_011514015.1:p.Glu3648Asp
XM_011515714.1:c.10983A>T (AKAP9) XP_011514016.1:p.Glu3661Asp
XM_011515716.1:c.10902A>T (AKAP9) XP_011514018.1:p.Glu3634Asp
XM_011515717.1:c.10857A>T (AKAP9) XP_011514019.1:p.Glu3619Asp
XM_011515718.1:c.10887A>T (AKAP9) XP_011514020.1:p.Glu3629Asp
XM_011515719.1:c.10863A>T (AKAP9) XP_011514021.1:p.Glu3621Asp
XM_011515721.1:c.5511A>T (AKAP9) XP_011514023.1:p.Glu1837Asp
XM_011515722.1:c.5472A>T (AKAP9) XP_011514024.1:p.Glu1824Asp
XM_017011642.2:c.10986A>T (AKAP9) XP_016867131.1:p.Glu3662Asp
XM_017011643.2:c.10947A>T (AKAP9) XP_016867132.1:p.Glu3649Asp
XM_017011644.2:c.10986A>T (AKAP9) XP_016867133.1:p.Glu3662Asp
XM_017011645.2:c.10932A>T (AKAP9) XP_016867134.1:p.Glu3644Asp
XM_017011646.2:c.10947A>T (AKAP9) XP_016867135.1:p.Glu3649Asp
XM_017011647.2:c.10893A>T (AKAP9) XP_016867136.1:p.Glu3631Asp
XM_017011648.2:c.10890A>T (AKAP9) XP_016867137.1:p.Glu3630Asp
XM_017011649.2:c.10923A>T (AKAP9) XP_016867138.1:p.Glu3641Asp
XM_017011650.2:c.10851A>T (AKAP9) XP_016867139.1:p.Glu3617Asp
XM_017011651.2:c.10845A>T (AKAP9) XP_016867140.1:p.Glu3615Asp
XM_017011652.2:c.10797A>T (AKAP9) XP_016867141.1:p.Glu3599Asp
XM_017011653.2:c.10758A>T (AKAP9) XP_016867142.1:p.Glu3586Asp
XM_017011654.2:c.10710A>T (AKAP9) XP_016867143.1:p.Glu3570Asp
XM_017011655.2:c.10614A>T (AKAP9) XP_016867144.1:p.Glu3538Asp
XM_017011656.2:c.10614A>T (AKAP9) XP_016867145.1:p.Glu3538Asp
XM_017011657.2:c.6651A>T (AKAP9) XP_016867146.1:p.Glu2217Asp
XM_017011658.2:c.5535A>T (AKAP9) XP_016867147.1:p.Glu1845Asp
XM_017011659.2:c.5496A>T (AKAP9) XP_016867148.1:p.Glu1832Asp
XM_017011660.2:c.5496A>T (AKAP9) XP_016867149.1:p.Glu1832Asp
XM_024446631.1:c.10749A>T (AKAP9) XP_024302399.1:p.Glu3583Asp
NM_147185.3:c.10827A>T (AKAP9) NP_671714.1:p.Glu3609Asp
NM_001379277.1:c.5496A>T (AKAP9) NP_001366206.1:p.Glu1832Asp
NM_005751.5:c.10851A>T (AKAP9) MANE Select NP_005742.4:p.Glu3617Asp