Canonical Allele Identifier: CA2474390612
Gene: CYP4A11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46932829G= , CM000663.2:g.46932829G= GRCh38
NC_000001.10:g.47398501G= , CM000663.1:g.47398501G= GRCh37
NC_000001.9:g.47171088G= NCBI36
NG_007932.1:g.13656C=

Transcript Alleles

HGVS Amino-acid change
ENST00000310638.9:c.1296C= MANE Select ENSP00000311095.4:p.Asp432=
ENST00000310638.8:c.1296C= ENSP00000311095.4:p.Asp432=
ENST00000371904.8:c.1299C= ENSP00000360971.4:p.Asp433=
ENST00000371905.1:c.1296C= ENSP00000360972.1:p.Asp432=
ENST00000462347.5:c.1002C= ENSP00000477495.1:p.Asp334=
ENST00000465874.5:c.*94C= ENSP00000476368.1:n.*94C=
ENST00000468629.5:c.*1C= ENSP00000476619.1:n.*1C=
ENST00000474458.5:c.*1C= ENSP00000476988.1:n.*1C=
ENST00000475477.5:c.*90C= ENSP00000476854.1:n.*90C=
NM_000778.3:c.1296C= NP_000769.2:p.Asp432=
XM_005270539.1:c.1002C= XP_005270596.1:p.Asp334=
XM_011540826.1:c.1314C= XP_011539128.1:p.Asp438=
XM_011540827.1:c.1020C= XP_011539129.1:p.Asp340=
XM_011540828.1:c.1002C= XP_011539130.1:p.Asp334=
XR_246241.1:n.1200C=
XR_246242.1:n.1184C=
NM_001319155.1:c.1200C= NP_001306084.1:p.Asp400=
NM_001363587.1:c.1002C= NP_001350516.1:p.Asp334=
NR_134988.1:n.1001C=
NR_134989.1:n.1192C=
NR_134990.1:n.1186C=
NR_134991.1:n.1173C=
NR_134992.1:n.802C=
NR_134993.1:n.936C=
NR_134994.1:n.1208C=
XM_017000465.1:c.984C= XP_016855954.1:p.Asp328=
XR_001737005.1:n.1274C=
NM_000778.4:c.1296C= MANE Select NP_000769.2:p.Asp432=
NM_001319155.2:c.1200C= NP_001306084.1:p.Asp400=
NM_001363587.2:c.1002C= NP_001350516.1:p.Asp334=
NR_134988.2:n.993C=
NR_134989.2:n.1184C=
NR_134990.2:n.1178C=
NR_134991.2:n.1165C=
NR_134992.2:n.794C=
NR_134993.2:n.928C=
NR_134994.2:n.1200C=