Canonical Allele Identifier: CA2474390508
Gene: CYP4A11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46932571G= , CM000663.2:g.46932571G= GRCh38
NC_000001.10:g.47398243G= , CM000663.1:g.47398243G= GRCh37
NC_000001.9:g.47170830G= NCBI36
NG_007932.1:g.13914C=

Transcript Alleles

HGVS Amino-acid change
ENST00000310638.9:c.1364+190C= MANE Select ENSP00000311095.4:n.1364+190C=
ENST00000310638.8:c.1364+190C= ENSP00000311095.4:n.1364+190C=
ENST00000371904.8:c.1367+190C= ENSP00000360971.4:n.1367+190C=
ENST00000371905.1:c.*186C= ENSP00000360972.1:n.*186C=
ENST00000462347.5:c.1070+190C= ENSP00000477495.1:n.1070+190C=
ENST00000465874.5:c.*352C= ENSP00000476368.1:n.*352C=
ENST00000468629.5:c.*69+190C= ENSP00000476619.1:n.*69+190C=
ENST00000474458.5:c.*69+190C= ENSP00000476988.1:n.*69+190C=
ENST00000475477.5:c.*158+190C= ENSP00000476854.1:n.*158+190C=
NM_000778.3:c.1364+190C= NP_000769.2:n.1364+190C=
XM_011540826.1:c.1382+190C= XP_011539128.1:n.1382+190C=
XM_011540827.1:c.1088+190C= XP_011539129.1:n.1088+190C=
XM_011540828.1:c.1070+190C= XP_011539130.1:n.1070+190C=
XR_246241.1:n.1268+190C=
XR_246242.1:n.1252+190C=
NM_001319155.1:c.1268+190C= NP_001306084.1:n.1268+190C=
NM_001363587.1:c.1070+190C= NP_001350516.1:n.1070+190C=
NR_134988.1:n.1069+190C=
NR_134989.1:n.1260+190C=
NR_134990.1:n.1254+190C=
NR_134991.1:n.1241+190C=
NR_134992.1:n.870+190C=
NR_134993.1:n.1004+190C=
NR_134994.1:n.1276+190C=
XM_017000465.1:c.1052+190C= XP_016855954.1:n.1052+190C=
XR_001737005.1:n.1342+190C=
NM_000778.4:c.1364+190C= MANE Select NP_000769.2:n.1364+190C=
NM_001319155.2:c.1268+190C= NP_001306084.1:n.1268+190C=
NM_001363587.2:c.1070+190C= NP_001350516.1:n.1070+190C=
NR_134988.2:n.1061+190C=
NR_134989.2:n.1252+190C=
NR_134990.2:n.1246+190C=
NR_134991.2:n.1233+190C=
NR_134992.2:n.862+190C=
NR_134993.2:n.996+190C=
NR_134994.2:n.1268+190C=