Canonical Allele Identifier: CA368158406

Gene: CYP51A1 AKAP9

Linked Data

• MyVariant Identifiers: chr7:g.91729032G>A (hg19) ; chr7:g.92099718G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92099718G>A , CM000669.2:g.92099718G>A	GRCh38
NC_000007.13:g.91729032G>A , CM000669.1:g.91729032G>A	GRCh37
NC_000007.12:g.91566968G>A	NCBI36
NG_011623.1:g.163844G>A , LRG_331:g.163844G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000691309.1:c.1352-14116C>T (CYP51A1)	ENSP00000510368.1:n.1352-14116C>T
ENST00000356239.8:c.10745G>A (AKAP9) MANE Select	ENSP00000348573.3:p.Gly3582Asp
ENST00000359028.7:c.10817G>A (AKAP9)	ENSP00000351922.4:p.Gly3606Asp
ENST00000394534.7:c.3737G>A (AKAP9)	ENSP00000378042.3:p.Gly1246Asp
ENST00000463118.2:n.93G>A (AKAP9)
ENST00000486313.2:c.233G>A (AKAP9)	ENSP00000505389.1:p.Gly78Asp
ENST00000487692.2:n.2823G>A (AKAP9)
ENST00000491695.2:c.5390G>A (AKAP9)	ENSP00000494626.2:p.Gly1797Asp
ENST00000679448.1:c.*1625G>A (AKAP9)	ENSP00000505889.1:n.*1625G>A
ENST00000679457.1:c.10721G>A (AKAP9)	ENSP00000505450.1:p.Gly3574Asp
ENST00000679474.1:n.10943G>A (AKAP9)
ENST00000679521.1:c.10691G>A (AKAP9)	ENSP00000505456.1:p.Gly3564Asp
ENST00000679821.1:c.10487G>A (AKAP9)	ENSP00000506040.1:p.Gly3496Asp
ENST00000680047.1:n.12415G>A (AKAP9)
ENST00000680072.1:c.10568G>A (AKAP9)	ENSP00000506581.1:p.Gly3523Asp
ENST00000680181.1:c.10652G>A (AKAP9)	ENSP00000505548.1:p.Gly3551Asp
ENST00000680365.1:c.4384G>A (AKAP9)	ENSP00000506019.1:n.4384G>A
ENST00000680513.1:c.10604G>A (AKAP9)	ENSP00000505284.1:p.Gly3535Asp
ENST00000680534.1:c.10784G>A (AKAP9)	ENSP00000506674.1:p.Gly3595Asp
ENST00000680766.1:c.10721G>A (AKAP9)	ENSP00000505204.1:p.Gly3574Asp
ENST00000680952.1:c.10721G>A (AKAP9)	ENSP00000506407.1:p.Gly3574Asp
ENST00000681216.1:c.4505G>A (AKAP9)	ENSP00000505551.1:n.4505G>A
ENST00000681412.1:c.10745G>A (AKAP9)	ENSP00000506486.1:p.Gly3582Asp
ENST00000681722.1:c.10721G>A (AKAP9)	ENSP00000506566.1:p.Gly3574Asp
ENST00000356239.7:c.10745G>A (AKAP9)	ENSP00000348573.3:p.Gly3582Asp
ENST00000359028.6:c.10754G>A (AKAP9)	ENSP00000351922.3:p.Gly3585Asp
ENST00000394534.6:c.4283G>A (AKAP9)	ENSP00000378042.2:p.Gly1428Asp
ENST00000463118.1:n.93G>A (AKAP9)
ENST00000487258.5:n.2495G>A (AKAP9)
ENST00000487692.1:n.545G>A (AKAP9)
NM_005751.4:c.10745G>A , LRG_331t1:c.10745G>A (AKAP9)	NP_005742.4:p.Gly3582Asp
NM_147185.2:c.10721G>A (AKAP9)	NP_671714.1:p.Gly3574Asp
XM_006715827.1:c.10604G>A (AKAP9)	XP_006715890.1:p.Gly3535Asp
XM_011515709.1:c.10892G>A (AKAP9)	XP_011514011.1:p.Gly3631Asp
XM_011515710.1:c.10916G>A (AKAP9)	XP_011514012.1:p.Gly3639Asp
XM_011515711.1:c.10856G>A (AKAP9)	XP_011514013.1:p.Gly3619Asp
XM_011515712.1:c.10853G>A (AKAP9)	XP_011514014.1:p.Gly3618Asp
XM_011515713.1:c.10838G>A (AKAP9)	XP_011514015.1:p.Gly3613Asp
XM_011515714.1:c.10877G>A (AKAP9)	XP_011514016.1:p.Gly3626Asp
XM_011515716.1:c.10796G>A (AKAP9)	XP_011514018.1:p.Gly3599Asp
XM_011515717.1:c.10751G>A (AKAP9)	XP_011514019.1:p.Gly3584Asp
XM_011515718.1:c.10781G>A (AKAP9)	XP_011514020.1:p.Gly3594Asp
XM_011515719.1:c.10757G>A (AKAP9)	XP_011514021.1:p.Gly3586Asp
XM_011515721.1:c.5405G>A (AKAP9)	XP_011514023.1:p.Gly1802Asp
XM_011515722.1:c.5366G>A (AKAP9)	XP_011514024.1:p.Gly1789Asp
XM_017011642.2:c.10880G>A (AKAP9)	XP_016867131.1:p.Gly3627Asp
XM_017011643.2:c.10841G>A (AKAP9)	XP_016867132.1:p.Gly3614Asp
XM_017011644.2:c.10880G>A (AKAP9)	XP_016867133.1:p.Gly3627Asp
XM_017011645.2:c.10826G>A (AKAP9)	XP_016867134.1:p.Gly3609Asp
XM_017011646.2:c.10841G>A (AKAP9)	XP_016867135.1:p.Gly3614Asp
XM_017011647.2:c.10787G>A (AKAP9)	XP_016867136.1:p.Gly3596Asp
XM_017011648.2:c.10784G>A (AKAP9)	XP_016867137.1:p.Gly3595Asp
XM_017011649.2:c.10817G>A (AKAP9)	XP_016867138.1:p.Gly3606Asp
XM_017011650.2:c.10745G>A (AKAP9)	XP_016867139.1:p.Gly3582Asp
XM_017011651.2:c.10739G>A (AKAP9)	XP_016867140.1:p.Gly3580Asp
XM_017011652.2:c.10691G>A (AKAP9)	XP_016867141.1:p.Gly3564Asp
XM_017011653.2:c.10652G>A (AKAP9)	XP_016867142.1:p.Gly3551Asp
XM_017011654.2:c.10604G>A (AKAP9)	XP_016867143.1:p.Gly3535Asp
XM_017011655.2:c.10508G>A (AKAP9)	XP_016867144.1:p.Gly3503Asp
XM_017011656.2:c.10508G>A (AKAP9)	XP_016867145.1:p.Gly3503Asp
XM_017011657.2:c.6545G>A (AKAP9)	XP_016867146.1:p.Gly2182Asp
XM_017011658.2:c.5429G>A (AKAP9)	XP_016867147.1:p.Gly1810Asp
XM_017011659.2:c.5390G>A (AKAP9)	XP_016867148.1:p.Gly1797Asp
XM_017011660.2:c.5390G>A (AKAP9)	XP_016867149.1:p.Gly1797Asp
XM_024446631.1:c.10643G>A (AKAP9)	XP_024302399.1:p.Gly3548Asp
NM_147185.3:c.10721G>A (AKAP9)	NP_671714.1:p.Gly3574Asp
NM_001379277.1:c.5390G>A (AKAP9)	NP_001366206.1:p.Gly1797Asp
NM_005751.5:c.10745G>A (AKAP9) MANE Select	NP_005742.4:p.Gly3582Asp