Canonical Allele Identifier: CA368158789

Gene: CYP51A1 AKAP9

Linked Data

• MyVariant Identifiers: chr7:g.91729106A>G (hg19) ; chr7:g.92099792A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92099792A>G , CM000669.2:g.92099792A>G	GRCh38
NC_000007.13:g.91729106A>G , CM000669.1:g.91729106A>G	GRCh37
NC_000007.12:g.91567042A>G	NCBI36
NG_011623.1:g.163918A>G , LRG_331:g.163918A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691309.1:c.1352-14190T>C (CYP51A1)	ENSP00000510368.1:n.1352-14190T>C
ENST00000356239.8:c.10819A>G (AKAP9) MANE Select	ENSP00000348573.3:p.Asn3607Asp
ENST00000359028.7:c.10891A>G (AKAP9)	ENSP00000351922.4:p.Asn3631Asp
ENST00000394534.7:c.3811A>G (AKAP9)	ENSP00000378042.3:p.Asn1271Asp
ENST00000463118.2:n.167A>G (AKAP9)
ENST00000486313.2:c.307A>G (AKAP9)	ENSP00000505389.1:p.Asn103Asp
ENST00000487692.2:n.2897A>G (AKAP9)
ENST00000491695.2:c.5464A>G (AKAP9)	ENSP00000494626.2:p.Asn1822Asp
ENST00000679448.1:c.*1699A>G (AKAP9)	ENSP00000505889.1:n.*1699A>G
ENST00000679457.1:c.10795A>G (AKAP9)	ENSP00000505450.1:p.Asn3599Asp
ENST00000679474.1:n.11017A>G (AKAP9)
ENST00000679521.1:c.10765A>G (AKAP9)	ENSP00000505456.1:p.Asn3589Asp
ENST00000679821.1:c.10561A>G (AKAP9)	ENSP00000506040.1:p.Asn3521Asp
ENST00000680047.1:n.12489A>G (AKAP9)
ENST00000680072.1:c.10642A>G (AKAP9)	ENSP00000506581.1:p.Asn3548Asp
ENST00000680181.1:c.10726A>G (AKAP9)	ENSP00000505548.1:p.Asn3576Asp
ENST00000680365.1:c.4458A>G (AKAP9)	ENSP00000506019.1:n.4458A>G
ENST00000680513.1:c.10678A>G (AKAP9)	ENSP00000505284.1:p.Asn3560Asp
ENST00000680534.1:c.10858A>G (AKAP9)	ENSP00000506674.1:p.Asn3620Asp
ENST00000680766.1:c.10795A>G (AKAP9)	ENSP00000505204.1:p.Asn3599Asp
ENST00000680952.1:c.10795A>G (AKAP9)	ENSP00000506407.1:p.Asn3599Asp
ENST00000681216.1:c.4579A>G (AKAP9)	ENSP00000505551.1:n.4579A>G
ENST00000681412.1:c.10819A>G (AKAP9)	ENSP00000506486.1:p.Asn3607Asp
ENST00000681722.1:c.10795A>G (AKAP9)	ENSP00000506566.1:p.Asn3599Asp
ENST00000356239.7:c.10819A>G (AKAP9)	ENSP00000348573.3:p.Asn3607Asp
ENST00000359028.6:c.10828A>G (AKAP9)	ENSP00000351922.3:p.Asn3610Asp
ENST00000394534.6:c.4357A>G (AKAP9)	ENSP00000378042.2:p.Asn1453Asp
ENST00000463118.1:n.167A>G (AKAP9)
ENST00000487258.5:n.2569A>G (AKAP9)
ENST00000487692.1:n.619A>G (AKAP9)
NM_005751.4:c.10819A>G , LRG_331t1:c.10819A>G (AKAP9)	NP_005742.4:p.Asn3607Asp
NM_147185.2:c.10795A>G (AKAP9)	NP_671714.1:p.Asn3599Asp
XM_006715827.1:c.10678A>G (AKAP9)	XP_006715890.1:p.Asn3560Asp
XM_011515709.1:c.10966A>G (AKAP9)	XP_011514011.1:p.Asn3656Asp
XM_011515710.1:c.10990A>G (AKAP9)	XP_011514012.1:p.Asn3664Asp
XM_011515711.1:c.10930A>G (AKAP9)	XP_011514013.1:p.Asn3644Asp
XM_011515712.1:c.10927A>G (AKAP9)	XP_011514014.1:p.Asn3643Asp
XM_011515713.1:c.10912A>G (AKAP9)	XP_011514015.1:p.Asn3638Asp
XM_011515714.1:c.10951A>G (AKAP9)	XP_011514016.1:p.Asn3651Asp
XM_011515716.1:c.10870A>G (AKAP9)	XP_011514018.1:p.Asn3624Asp
XM_011515717.1:c.10825A>G (AKAP9)	XP_011514019.1:p.Asn3609Asp
XM_011515718.1:c.10855A>G (AKAP9)	XP_011514020.1:p.Asn3619Asp
XM_011515719.1:c.10831A>G (AKAP9)	XP_011514021.1:p.Asn3611Asp
XM_011515721.1:c.5479A>G (AKAP9)	XP_011514023.1:p.Asn1827Asp
XM_011515722.1:c.5440A>G (AKAP9)	XP_011514024.1:p.Asn1814Asp
XM_017011642.2:c.10954A>G (AKAP9)	XP_016867131.1:p.Asn3652Asp
XM_017011643.2:c.10915A>G (AKAP9)	XP_016867132.1:p.Asn3639Asp
XM_017011644.2:c.10954A>G (AKAP9)	XP_016867133.1:p.Asn3652Asp
XM_017011645.2:c.10900A>G (AKAP9)	XP_016867134.1:p.Asn3634Asp
XM_017011646.2:c.10915A>G (AKAP9)	XP_016867135.1:p.Asn3639Asp
XM_017011647.2:c.10861A>G (AKAP9)	XP_016867136.1:p.Asn3621Asp
XM_017011648.2:c.10858A>G (AKAP9)	XP_016867137.1:p.Asn3620Asp
XM_017011649.2:c.10891A>G (AKAP9)	XP_016867138.1:p.Asn3631Asp
XM_017011650.2:c.10819A>G (AKAP9)	XP_016867139.1:p.Asn3607Asp
XM_017011651.2:c.10813A>G (AKAP9)	XP_016867140.1:p.Asn3605Asp
XM_017011652.2:c.10765A>G (AKAP9)	XP_016867141.1:p.Asn3589Asp
XM_017011653.2:c.10726A>G (AKAP9)	XP_016867142.1:p.Asn3576Asp
XM_017011654.2:c.10678A>G (AKAP9)	XP_016867143.1:p.Asn3560Asp
XM_017011655.2:c.10582A>G (AKAP9)	XP_016867144.1:p.Asn3528Asp
XM_017011656.2:c.10582A>G (AKAP9)	XP_016867145.1:p.Asn3528Asp
XM_017011657.2:c.6619A>G (AKAP9)	XP_016867146.1:p.Asn2207Asp
XM_017011658.2:c.5503A>G (AKAP9)	XP_016867147.1:p.Asn1835Asp
XM_017011659.2:c.5464A>G (AKAP9)	XP_016867148.1:p.Asn1822Asp
XM_017011660.2:c.5464A>G (AKAP9)	XP_016867149.1:p.Asn1822Asp
XM_024446631.1:c.10717A>G (AKAP9)	XP_024302399.1:p.Asn3573Asp
NM_147185.3:c.10795A>G (AKAP9)	NP_671714.1:p.Asn3599Asp
NM_001379277.1:c.5464A>G (AKAP9)	NP_001366206.1:p.Asn1822Asp
NM_005751.5:c.10819A>G (AKAP9) MANE Select	NP_005742.4:p.Asn3607Asp