Canonical Allele Identifier: CA2474390531
Gene: CYP4A11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46932633C= , CM000663.2:g.46932633C= GRCh38
NC_000001.10:g.47398305C= , CM000663.1:g.47398305C= GRCh37
NC_000001.9:g.47170892C= NCBI36
NG_007932.1:g.13852G=

Transcript Alleles

HGVS Amino-acid change
ENST00000310638.9:c.1364+128G= MANE Select ENSP00000311095.4:n.1364+128G=
ENST00000310638.8:c.1364+128G= ENSP00000311095.4:n.1364+128G=
ENST00000371904.8:c.1367+128G= ENSP00000360971.4:n.1367+128G=
ENST00000371905.1:c.*124G= ENSP00000360972.1:n.*124G=
ENST00000462347.5:c.1070+128G= ENSP00000477495.1:n.1070+128G=
ENST00000465874.5:c.*290G= ENSP00000476368.1:n.*290G=
ENST00000468629.5:c.*69+128G= ENSP00000476619.1:n.*69+128G=
ENST00000474458.5:c.*69+128G= ENSP00000476988.1:n.*69+128G=
ENST00000475477.5:c.*158+128G= ENSP00000476854.1:n.*158+128G=
NM_000778.3:c.1364+128G= NP_000769.2:n.1364+128G=
XM_011540826.1:c.1382+128G= XP_011539128.1:n.1382+128G=
XM_011540827.1:c.1088+128G= XP_011539129.1:n.1088+128G=
XM_011540828.1:c.1070+128G= XP_011539130.1:n.1070+128G=
XR_246241.1:n.1268+128G=
XR_246242.1:n.1252+128G=
NM_001319155.1:c.1268+128G= NP_001306084.1:n.1268+128G=
NM_001363587.1:c.1070+128G= NP_001350516.1:n.1070+128G=
NR_134988.1:n.1069+128G=
NR_134989.1:n.1260+128G=
NR_134990.1:n.1254+128G=
NR_134991.1:n.1241+128G=
NR_134992.1:n.870+128G=
NR_134993.1:n.1004+128G=
NR_134994.1:n.1276+128G=
XM_017000465.1:c.1052+128G= XP_016855954.1:n.1052+128G=
XR_001737005.1:n.1342+128G=
NM_000778.4:c.1364+128G= MANE Select NP_000769.2:n.1364+128G=
NM_001319155.2:c.1268+128G= NP_001306084.1:n.1268+128G=
NM_001363587.2:c.1070+128G= NP_001350516.1:n.1070+128G=
NR_134988.2:n.1061+128G=
NR_134989.2:n.1252+128G=
NR_134990.2:n.1246+128G=
NR_134991.2:n.1233+128G=
NR_134992.2:n.862+128G=
NR_134993.2:n.996+128G=
NR_134994.2:n.1268+128G=