Canonical Allele Identifier: CA2474390693
Gene: CYP4A11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46932984T= , CM000663.2:g.46932984T= GRCh38
NC_000001.10:g.47398656T= , CM000663.1:g.47398656T= GRCh37
NC_000001.9:g.47171243T= NCBI36
NG_007932.1:g.13501A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000310638.9:c.1286A= MANE Select ENSP00000311095.4:p.Glu429=
ENST00000310638.8:c.1286A= ENSP00000311095.4:p.Glu429=
ENST00000371904.8:c.1289A= ENSP00000360971.4:p.Glu430=
ENST00000371905.1:c.1286A= ENSP00000360972.1:p.Glu429=
ENST00000462347.5:c.992A= ENSP00000477495.1:p.Glu331=
ENST00000465874.5:c.*84A= ENSP00000476368.1:n.*84A=
ENST00000468629.5:c.1127-147A= ENSP00000476619.1:n.1127-147A=
ENST00000474458.5:c.743-147A= ENSP00000476988.1:n.743-147A=
ENST00000475477.5:c.*82-147A= ENSP00000476854.1:n.*82-147A=
NM_000778.3:c.1286A= NP_000769.2:p.Glu429=
XM_005270539.1:c.992A= XP_005270596.1:p.Glu331=
XM_011540826.1:c.1304A= XP_011539128.1:p.Glu435=
XM_011540827.1:c.1010A= XP_011539129.1:p.Glu337=
XM_011540828.1:c.992A= XP_011539130.1:p.Glu331=
XR_246241.1:n.1190A=
XR_246242.1:n.1174A=
NM_001319155.1:c.1190A= NP_001306084.1:p.Glu397=
NM_001363587.1:c.992A= NP_001350516.1:p.Glu331=
NR_134988.1:n.991A=
NR_134989.1:n.1182A=
NR_134990.1:n.1178-147A=
NR_134991.1:n.1163A=
NR_134992.1:n.794-147A=
NR_134993.1:n.928-147A=
NR_134994.1:n.1198A=
XM_017000465.1:c.974A= XP_016855954.1:p.Glu325=
XR_001737005.1:n.1266-147A=
NM_000778.4:c.1286A= MANE Select NP_000769.2:p.Glu429=
NM_001319155.2:c.1190A= NP_001306084.1:p.Glu397=
NM_001363587.2:c.992A= NP_001350516.1:p.Glu331=
NR_134988.2:n.983A=
NR_134989.2:n.1174A=
NR_134990.2:n.1170-147A=
NR_134991.2:n.1155A=
NR_134992.2:n.786-147A=
NR_134993.2:n.920-147A=
NR_134994.2:n.1190A=