Canonical Allele Identifier: CA456454131
Gene: CYP51A1 HGNC NCBI
AKAP9 HGNC NCBI

Linked Data

gnomAD v4: 7-92099732-A-C
MyVariant Identifiers: chr7:g.91729046A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92099732A>C , CM000669.2:g.92099732A>C GRCh38
NC_000007.13:g.91729046A>C , CM000669.1:g.91729046A>C GRCh37
NC_000007.12:g.91566982A>C NCBI36
NG_011623.1:g.163858A>C , LRG_331:g.163858A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000691309.1:c.1352-14130T>G (CYP51A1) ENSP00000510368.1:n.1352-14130T>G
ENST00000356239.8:c.10759A>C (AKAP9) MANE Select ENSP00000348573.3:p.Arg3587=
ENST00000359028.7:c.10831A>C (AKAP9) ENSP00000351922.4:p.Arg3611=
ENST00000394534.7:c.3751A>C (AKAP9) ENSP00000378042.3:p.Arg1251=
ENST00000463118.2:n.107A>C (AKAP9)
ENST00000486313.2:c.247A>C (AKAP9) ENSP00000505389.1:p.Arg83=
ENST00000487692.2:n.2837A>C (AKAP9)
ENST00000491695.2:c.5404A>C (AKAP9) ENSP00000494626.2:p.Arg1802=
ENST00000679448.1:c.*1639A>C (AKAP9) ENSP00000505889.1:n.*1639A>C
ENST00000679457.1:c.10735A>C (AKAP9) ENSP00000505450.1:p.Arg3579=
ENST00000679474.1:n.10957A>C (AKAP9)
ENST00000679521.1:c.10705A>C (AKAP9) ENSP00000505456.1:p.Arg3569=
ENST00000679821.1:c.10501A>C (AKAP9) ENSP00000506040.1:p.Arg3501=
ENST00000680047.1:n.12429A>C (AKAP9)
ENST00000680072.1:c.10582A>C (AKAP9) ENSP00000506581.1:p.Arg3528=
ENST00000680181.1:c.10666A>C (AKAP9) ENSP00000505548.1:p.Arg3556=
ENST00000680365.1:c.4398A>C (AKAP9) ENSP00000506019.1:n.4398A>C
ENST00000680513.1:c.10618A>C (AKAP9) ENSP00000505284.1:p.Arg3540=
ENST00000680534.1:c.10798A>C (AKAP9) ENSP00000506674.1:p.Arg3600=
ENST00000680766.1:c.10735A>C (AKAP9) ENSP00000505204.1:p.Arg3579=
ENST00000680952.1:c.10735A>C (AKAP9) ENSP00000506407.1:p.Arg3579=
ENST00000681216.1:c.4519A>C (AKAP9) ENSP00000505551.1:n.4519A>C
ENST00000681412.1:c.10759A>C (AKAP9) ENSP00000506486.1:p.Arg3587=
ENST00000681722.1:c.10735A>C (AKAP9) ENSP00000506566.1:p.Arg3579=
ENST00000356239.7:c.10759A>C (AKAP9) ENSP00000348573.3:p.Arg3587=
ENST00000359028.6:c.10768A>C (AKAP9) ENSP00000351922.3:p.Arg3590=
ENST00000394534.6:c.4297A>C (AKAP9) ENSP00000378042.2:p.Arg1433=
ENST00000463118.1:n.107A>C (AKAP9)
ENST00000487258.5:n.2509A>C (AKAP9)
ENST00000487692.1:n.559A>C (AKAP9)
NM_005751.4:c.10759A>C , LRG_331t1:c.10759A>C (AKAP9) NP_005742.4:p.Arg3587=
NM_147185.2:c.10735A>C (AKAP9) NP_671714.1:p.Arg3579=
XM_006715827.1:c.10618A>C (AKAP9) XP_006715890.1:p.Arg3540=
XM_011515709.1:c.10906A>C (AKAP9) XP_011514011.1:p.Arg3636=
XM_011515710.1:c.10930A>C (AKAP9) XP_011514012.1:p.Arg3644=
XM_011515711.1:c.10870A>C (AKAP9) XP_011514013.1:p.Arg3624=
XM_011515712.1:c.10867A>C (AKAP9) XP_011514014.1:p.Arg3623=
XM_011515713.1:c.10852A>C (AKAP9) XP_011514015.1:p.Arg3618=
XM_011515714.1:c.10891A>C (AKAP9) XP_011514016.1:p.Arg3631=
XM_011515716.1:c.10810A>C (AKAP9) XP_011514018.1:p.Arg3604=
XM_011515717.1:c.10765A>C (AKAP9) XP_011514019.1:p.Arg3589=
XM_011515718.1:c.10795A>C (AKAP9) XP_011514020.1:p.Arg3599=
XM_011515719.1:c.10771A>C (AKAP9) XP_011514021.1:p.Arg3591=
XM_011515721.1:c.5419A>C (AKAP9) XP_011514023.1:p.Arg1807=
XM_011515722.1:c.5380A>C (AKAP9) XP_011514024.1:p.Arg1794=
XM_017011642.2:c.10894A>C (AKAP9) XP_016867131.1:p.Arg3632=
XM_017011643.2:c.10855A>C (AKAP9) XP_016867132.1:p.Arg3619=
XM_017011644.2:c.10894A>C (AKAP9) XP_016867133.1:p.Arg3632=
XM_017011645.2:c.10840A>C (AKAP9) XP_016867134.1:p.Arg3614=
XM_017011646.2:c.10855A>C (AKAP9) XP_016867135.1:p.Arg3619=
XM_017011647.2:c.10801A>C (AKAP9) XP_016867136.1:p.Arg3601=
XM_017011648.2:c.10798A>C (AKAP9) XP_016867137.1:p.Arg3600=
XM_017011649.2:c.10831A>C (AKAP9) XP_016867138.1:p.Arg3611=
XM_017011650.2:c.10759A>C (AKAP9) XP_016867139.1:p.Arg3587=
XM_017011651.2:c.10753A>C (AKAP9) XP_016867140.1:p.Arg3585=
XM_017011652.2:c.10705A>C (AKAP9) XP_016867141.1:p.Arg3569=
XM_017011653.2:c.10666A>C (AKAP9) XP_016867142.1:p.Arg3556=
XM_017011654.2:c.10618A>C (AKAP9) XP_016867143.1:p.Arg3540=
XM_017011655.2:c.10522A>C (AKAP9) XP_016867144.1:p.Arg3508=
XM_017011656.2:c.10522A>C (AKAP9) XP_016867145.1:p.Arg3508=
XM_017011657.2:c.6559A>C (AKAP9) XP_016867146.1:p.Arg2187=
XM_017011658.2:c.5443A>C (AKAP9) XP_016867147.1:p.Arg1815=
XM_017011659.2:c.5404A>C (AKAP9) XP_016867148.1:p.Arg1802=
XM_017011660.2:c.5404A>C (AKAP9) XP_016867149.1:p.Arg1802=
XM_024446631.1:c.10657A>C (AKAP9) XP_024302399.1:p.Arg3553=
NM_147185.3:c.10735A>C (AKAP9) NP_671714.1:p.Arg3579=
NM_001379277.1:c.5404A>C (AKAP9) NP_001366206.1:p.Arg1802=
NM_005751.5:c.10759A>C (AKAP9) MANE Select NP_005742.4:p.Arg3587=