Canonical Allele Identifier: CA1139851961
Gene: CYP4A11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46932824A= , CM000663.2:g.46932824A= GRCh38
NC_000001.10:g.47398496A= , CM000663.1:g.47398496A= GRCh37
NC_000001.9:g.47171083A= NCBI36
NG_007932.1:g.13661T=

Transcript Alleles

HGVS Amino-acid change
ENST00000310638.9:c.1301T= MANE Select ENSP00000311095.4:p.Phe434=
ENST00000310638.8:c.1301T= ENSP00000311095.4:p.Phe434=
ENST00000371904.8:c.1304T= ENSP00000360971.4:p.Phe435=
ENST00000371905.1:c.1301T= ENSP00000360972.1:p.Phe434=
ENST00000462347.5:c.1007T= ENSP00000477495.1:p.Phe336=
ENST00000465874.5:c.*99T= ENSP00000476368.1:n.*99T=
ENST00000468629.5:c.*6T= ENSP00000476619.1:n.*6T=
ENST00000474458.5:c.*6T= ENSP00000476988.1:n.*6T=
ENST00000475477.5:c.*95T= ENSP00000476854.1:n.*95T=
NM_000778.3:c.1301T= NP_000769.2:p.Phe434=
XM_005270539.1:c.1007T= XP_005270596.1:p.Phe336=
XM_011540826.1:c.1319T= XP_011539128.1:p.Phe440=
XM_011540827.1:c.1025T= XP_011539129.1:p.Phe342=
XM_011540828.1:c.1007T= XP_011539130.1:p.Phe336=
XR_246241.1:n.1205T=
XR_246242.1:n.1189T=
NM_001319155.1:c.1205T= NP_001306084.1:p.Phe402=
NM_001363587.1:c.1007T= NP_001350516.1:p.Phe336=
NR_134988.1:n.1006T=
NR_134989.1:n.1197T=
NR_134990.1:n.1191T=
NR_134991.1:n.1178T=
NR_134992.1:n.807T=
NR_134993.1:n.941T=
NR_134994.1:n.1213T=
XM_017000465.1:c.989T= XP_016855954.1:p.Phe330=
XR_001737005.1:n.1279T=
NM_000778.4:c.1301T= MANE Select NP_000769.2:p.Phe434=
NM_001319155.2:c.1205T= NP_001306084.1:p.Phe402=
NM_001363587.2:c.1007T= NP_001350516.1:p.Phe336=
NR_134988.2:n.998T=
NR_134989.2:n.1189T=
NR_134990.2:n.1183T=
NR_134991.2:n.1170T=
NR_134992.2:n.799T=
NR_134993.2:n.933T=
NR_134994.2:n.1205T=