Canonical Allele Identifier: CA340223215

Gene: CYP4A11

Linked Data

• MyVariant Identifiers: chr1:g.47398491A>T (hg19) ; chr1:g.46932819A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932819A>T , CM000663.2:g.46932819A>T	GRCh38
NC_000001.10:g.47398491A>T , CM000663.1:g.47398491A>T	GRCh37
NC_000001.9:g.47171078A>T	NCBI36
NG_007932.1:g.13666T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1306T>A MANE Select	ENSP00000311095.4:p.Phe436Ile
ENST00000310638.8:c.1306T>A	ENSP00000311095.4:p.Phe436Ile
ENST00000371904.8:c.1309T>A	ENSP00000360971.4:p.Phe437Ile
ENST00000371905.1:c.1306T>A	ENSP00000360972.1:p.Phe436Ile
ENST00000462347.5:c.1012T>A	ENSP00000477495.1:p.Phe338Ile
ENST00000465874.5:c.*104T>A	ENSP00000476368.1:n.*104T>A
ENST00000468629.5:c.*11T>A	ENSP00000476619.1:n.*11T>A
ENST00000474458.5:c.*11T>A	ENSP00000476988.1:n.*11T>A
ENST00000475477.5:c.*100T>A	ENSP00000476854.1:n.*100T>A
NM_000778.3:c.1306T>A	NP_000769.2:p.Phe436Ile
XM_005270539.1:c.1012T>A	XP_005270596.1:p.Phe338Ile
XM_011540826.1:c.1324T>A	XP_011539128.1:p.Phe442Ile
XM_011540827.1:c.1030T>A	XP_011539129.1:p.Phe344Ile
XM_011540828.1:c.1012T>A	XP_011539130.1:p.Phe338Ile
XR_246241.1:n.1210T>A
XR_246242.1:n.1194T>A
NM_001319155.1:c.1210T>A	NP_001306084.1:p.Phe404Ile
NM_001363587.1:c.1012T>A	NP_001350516.1:p.Phe338Ile
NR_134988.1:n.1011T>A
NR_134989.1:n.1202T>A
NR_134990.1:n.1196T>A
NR_134991.1:n.1183T>A
NR_134992.1:n.812T>A
NR_134993.1:n.946T>A
NR_134994.1:n.1218T>A
XM_017000465.1:c.994T>A	XP_016855954.1:p.Phe332Ile
XR_001737005.1:n.1284T>A
NM_000778.4:c.1306T>A MANE Select	NP_000769.2:p.Phe436Ile
NM_001319155.2:c.1210T>A	NP_001306084.1:p.Phe404Ile
NM_001363587.2:c.1012T>A	NP_001350516.1:p.Phe338Ile
NR_134988.2:n.1003T>A
NR_134989.2:n.1194T>A
NR_134990.2:n.1188T>A
NR_134991.2:n.1175T>A
NR_134992.2:n.804T>A
NR_134993.2:n.938T>A
NR_134994.2:n.1210T>A