Canonical Allele Identifier: CA417755794

Gene: CYP4A11

Linked Data

• MyVariant Identifiers: chr1:g.47398459A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932787A>T , CM000663.2:g.46932787A>T	GRCh38
NC_000001.10:g.47398459A>T , CM000663.1:g.47398459A>T	GRCh37
NC_000001.9:g.47171046A>T	NCBI36
NG_007932.1:g.13698T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1338T>A MANE Select	ENSP00000311095.4:p.Ala446=
ENST00000310638.8:c.1338T>A	ENSP00000311095.4:p.Ala446=
ENST00000371904.8:c.1341T>A	ENSP00000360971.4:p.Ala447=
ENST00000371905.1:c.1338T>A	ENSP00000360972.1:p.Ala446=
ENST00000462347.5:c.1044T>A	ENSP00000477495.1:p.Ala348=
ENST00000465874.5:c.*136T>A	ENSP00000476368.1:n.*136T>A
ENST00000468629.5:c.*43T>A	ENSP00000476619.1:n.*43T>A
ENST00000474458.5:c.*43T>A	ENSP00000476988.1:n.*43T>A
ENST00000475477.5:c.*132T>A	ENSP00000476854.1:n.*132T>A
NM_000778.3:c.1338T>A	NP_000769.2:p.Ala446=
XM_005270539.1:c.1044T>A	XP_005270596.1:p.Ala348=
XM_011540826.1:c.1356T>A	XP_011539128.1:p.Ala452=
XM_011540827.1:c.1062T>A	XP_011539129.1:p.Ala354=
XM_011540828.1:c.1044T>A	XP_011539130.1:p.Ala348=
XR_246241.1:n.1242T>A
XR_246242.1:n.1226T>A
NM_001319155.1:c.1242T>A	NP_001306084.1:p.Ala414=
NM_001363587.1:c.1044T>A	NP_001350516.1:p.Ala348=
NR_134988.1:n.1043T>A
NR_134989.1:n.1234T>A
NR_134990.1:n.1228T>A
NR_134991.1:n.1215T>A
NR_134992.1:n.844T>A
NR_134993.1:n.978T>A
NR_134994.1:n.1250T>A
XM_017000465.1:c.1026T>A	XP_016855954.1:p.Ala342=
XR_001737005.1:n.1316T>A
NM_000778.4:c.1338T>A MANE Select	NP_000769.2:p.Ala446=
NM_001319155.2:c.1242T>A	NP_001306084.1:p.Ala414=
NM_001363587.2:c.1044T>A	NP_001350516.1:p.Ala348=
NR_134988.2:n.1035T>A
NR_134989.2:n.1226T>A
NR_134990.2:n.1220T>A
NR_134991.2:n.1207T>A
NR_134992.2:n.836T>A
NR_134993.2:n.970T>A
NR_134994.2:n.1242T>A