Canonical Allele Identifier: CA340223210

Gene: CYP4A11

Linked Data

• MyVariant Identifiers: chr1:g.47398489A>T (hg19) ; chr1:g.46932817A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932817A>T , CM000663.2:g.46932817A>T	GRCh38
NC_000001.10:g.47398489A>T , CM000663.1:g.47398489A>T	GRCh37
NC_000001.9:g.47171076A>T	NCBI36
NG_007932.1:g.13668T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1308T>A MANE Select	ENSP00000311095.4:p.Phe436Leu
ENST00000310638.8:c.1308T>A	ENSP00000311095.4:p.Phe436Leu
ENST00000371904.8:c.1311T>A	ENSP00000360971.4:p.Phe437Leu
ENST00000371905.1:c.1308T>A	ENSP00000360972.1:p.Phe436Leu
ENST00000462347.5:c.1014T>A	ENSP00000477495.1:p.Phe338Leu
ENST00000465874.5:c.*106T>A	ENSP00000476368.1:n.*106T>A
ENST00000468629.5:c.*13T>A	ENSP00000476619.1:n.*13T>A
ENST00000474458.5:c.*13T>A	ENSP00000476988.1:n.*13T>A
ENST00000475477.5:c.*102T>A	ENSP00000476854.1:n.*102T>A
NM_000778.3:c.1308T>A	NP_000769.2:p.Phe436Leu
XM_005270539.1:c.1014T>A	XP_005270596.1:p.Phe338Leu
XM_011540826.1:c.1326T>A	XP_011539128.1:p.Phe442Leu
XM_011540827.1:c.1032T>A	XP_011539129.1:p.Phe344Leu
XM_011540828.1:c.1014T>A	XP_011539130.1:p.Phe338Leu
XR_246241.1:n.1212T>A
XR_246242.1:n.1196T>A
NM_001319155.1:c.1212T>A	NP_001306084.1:p.Phe404Leu
NM_001363587.1:c.1014T>A	NP_001350516.1:p.Phe338Leu
NR_134988.1:n.1013T>A
NR_134989.1:n.1204T>A
NR_134990.1:n.1198T>A
NR_134991.1:n.1185T>A
NR_134992.1:n.814T>A
NR_134993.1:n.948T>A
NR_134994.1:n.1220T>A
XM_017000465.1:c.996T>A	XP_016855954.1:p.Phe332Leu
XR_001737005.1:n.1286T>A
NM_000778.4:c.1308T>A MANE Select	NP_000769.2:p.Phe436Leu
NM_001319155.2:c.1212T>A	NP_001306084.1:p.Phe404Leu
NM_001363587.2:c.1014T>A	NP_001350516.1:p.Phe338Leu
NR_134988.2:n.1005T>A
NR_134989.2:n.1196T>A
NR_134990.2:n.1190T>A
NR_134991.2:n.1177T>A
NR_134992.2:n.806T>A
NR_134993.2:n.940T>A
NR_134994.2:n.1212T>A