Canonical Allele Identifier: CA456454135
Gene: CYP51A1 HGNC NCBI
AKAP9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.91729051A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92099737A>T , CM000669.2:g.92099737A>T GRCh38
NC_000007.13:g.91729051A>T , CM000669.1:g.91729051A>T GRCh37
NC_000007.12:g.91566987A>T NCBI36
NG_011623.1:g.163863A>T , LRG_331:g.163863A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000691309.1:c.1352-14135T>A (CYP51A1) ENSP00000510368.1:n.1352-14135T>A
ENST00000356239.8:c.10764A>T (AKAP9) MANE Select ENSP00000348573.3:p.Leu3588=
ENST00000359028.7:c.10836A>T (AKAP9) ENSP00000351922.4:p.Leu3612=
ENST00000394534.7:c.3756A>T (AKAP9) ENSP00000378042.3:p.Leu1252=
ENST00000463118.2:n.112A>T (AKAP9)
ENST00000486313.2:c.252A>T (AKAP9) ENSP00000505389.1:p.Leu84=
ENST00000487692.2:n.2842A>T (AKAP9)
ENST00000491695.2:c.5409A>T (AKAP9) ENSP00000494626.2:p.Leu1803=
ENST00000679448.1:c.*1644A>T (AKAP9) ENSP00000505889.1:n.*1644A>T
ENST00000679457.1:c.10740A>T (AKAP9) ENSP00000505450.1:p.Leu3580=
ENST00000679474.1:n.10962A>T (AKAP9)
ENST00000679521.1:c.10710A>T (AKAP9) ENSP00000505456.1:p.Leu3570=
ENST00000679821.1:c.10506A>T (AKAP9) ENSP00000506040.1:p.Leu3502=
ENST00000680047.1:n.12434A>T (AKAP9)
ENST00000680072.1:c.10587A>T (AKAP9) ENSP00000506581.1:p.Leu3529=
ENST00000680181.1:c.10671A>T (AKAP9) ENSP00000505548.1:p.Leu3557=
ENST00000680365.1:c.4403A>T (AKAP9) ENSP00000506019.1:n.4403A>T
ENST00000680513.1:c.10623A>T (AKAP9) ENSP00000505284.1:p.Leu3541=
ENST00000680534.1:c.10803A>T (AKAP9) ENSP00000506674.1:p.Leu3601=
ENST00000680766.1:c.10740A>T (AKAP9) ENSP00000505204.1:p.Leu3580=
ENST00000680952.1:c.10740A>T (AKAP9) ENSP00000506407.1:p.Leu3580=
ENST00000681216.1:c.4524A>T (AKAP9) ENSP00000505551.1:n.4524A>T
ENST00000681412.1:c.10764A>T (AKAP9) ENSP00000506486.1:p.Leu3588=
ENST00000681722.1:c.10740A>T (AKAP9) ENSP00000506566.1:p.Leu3580=
ENST00000356239.7:c.10764A>T (AKAP9) ENSP00000348573.3:p.Leu3588=
ENST00000359028.6:c.10773A>T (AKAP9) ENSP00000351922.3:p.Leu3591=
ENST00000394534.6:c.4302A>T (AKAP9) ENSP00000378042.2:p.Leu1434=
ENST00000463118.1:n.112A>T (AKAP9)
ENST00000487258.5:n.2514A>T (AKAP9)
ENST00000487692.1:n.564A>T (AKAP9)
NM_005751.4:c.10764A>T , LRG_331t1:c.10764A>T (AKAP9) NP_005742.4:p.Leu3588=
NM_147185.2:c.10740A>T (AKAP9) NP_671714.1:p.Leu3580=
XM_006715827.1:c.10623A>T (AKAP9) XP_006715890.1:p.Leu3541=
XM_011515709.1:c.10911A>T (AKAP9) XP_011514011.1:p.Leu3637=
XM_011515710.1:c.10935A>T (AKAP9) XP_011514012.1:p.Leu3645=
XM_011515711.1:c.10875A>T (AKAP9) XP_011514013.1:p.Leu3625=
XM_011515712.1:c.10872A>T (AKAP9) XP_011514014.1:p.Leu3624=
XM_011515713.1:c.10857A>T (AKAP9) XP_011514015.1:p.Leu3619=
XM_011515714.1:c.10896A>T (AKAP9) XP_011514016.1:p.Leu3632=
XM_011515716.1:c.10815A>T (AKAP9) XP_011514018.1:p.Leu3605=
XM_011515717.1:c.10770A>T (AKAP9) XP_011514019.1:p.Leu3590=
XM_011515718.1:c.10800A>T (AKAP9) XP_011514020.1:p.Leu3600=
XM_011515719.1:c.10776A>T (AKAP9) XP_011514021.1:p.Leu3592=
XM_011515721.1:c.5424A>T (AKAP9) XP_011514023.1:p.Leu1808=
XM_011515722.1:c.5385A>T (AKAP9) XP_011514024.1:p.Leu1795=
XM_017011642.2:c.10899A>T (AKAP9) XP_016867131.1:p.Leu3633=
XM_017011643.2:c.10860A>T (AKAP9) XP_016867132.1:p.Leu3620=
XM_017011644.2:c.10899A>T (AKAP9) XP_016867133.1:p.Leu3633=
XM_017011645.2:c.10845A>T (AKAP9) XP_016867134.1:p.Leu3615=
XM_017011646.2:c.10860A>T (AKAP9) XP_016867135.1:p.Leu3620=
XM_017011647.2:c.10806A>T (AKAP9) XP_016867136.1:p.Leu3602=
XM_017011648.2:c.10803A>T (AKAP9) XP_016867137.1:p.Leu3601=
XM_017011649.2:c.10836A>T (AKAP9) XP_016867138.1:p.Leu3612=
XM_017011650.2:c.10764A>T (AKAP9) XP_016867139.1:p.Leu3588=
XM_017011651.2:c.10758A>T (AKAP9) XP_016867140.1:p.Leu3586=
XM_017011652.2:c.10710A>T (AKAP9) XP_016867141.1:p.Leu3570=
XM_017011653.2:c.10671A>T (AKAP9) XP_016867142.1:p.Leu3557=
XM_017011654.2:c.10623A>T (AKAP9) XP_016867143.1:p.Leu3541=
XM_017011655.2:c.10527A>T (AKAP9) XP_016867144.1:p.Leu3509=
XM_017011656.2:c.10527A>T (AKAP9) XP_016867145.1:p.Leu3509=
XM_017011657.2:c.6564A>T (AKAP9) XP_016867146.1:p.Leu2188=
XM_017011658.2:c.5448A>T (AKAP9) XP_016867147.1:p.Leu1816=
XM_017011659.2:c.5409A>T (AKAP9) XP_016867148.1:p.Leu1803=
XM_017011660.2:c.5409A>T (AKAP9) XP_016867149.1:p.Leu1803=
XM_024446631.1:c.10662A>T (AKAP9) XP_024302399.1:p.Leu3554=
NM_147185.3:c.10740A>T (AKAP9) NP_671714.1:p.Leu3580=
NM_001379277.1:c.5409A>T (AKAP9) NP_001366206.1:p.Leu1803=
NM_005751.5:c.10764A>T (AKAP9) MANE Select NP_005742.4:p.Leu3588=