Canonical Allele Identifier: CA2474390598
Gene: CYP4A11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46932790G= , CM000663.2:g.46932790G= GRCh38
NC_000001.10:g.47398462G= , CM000663.1:g.47398462G= GRCh37
NC_000001.9:g.47171049G= NCBI36
NG_007932.1:g.13695C=

Transcript Alleles

HGVS Amino-acid change
ENST00000310638.9:c.1335C= MANE Select ENSP00000311095.4:p.His445=
ENST00000310638.8:c.1335C= ENSP00000311095.4:p.His445=
ENST00000371904.8:c.1338C= ENSP00000360971.4:p.His446=
ENST00000371905.1:c.1335C= ENSP00000360972.1:p.His445=
ENST00000462347.5:c.1041C= ENSP00000477495.1:p.His347=
ENST00000465874.5:c.*133C= ENSP00000476368.1:n.*133C=
ENST00000468629.5:c.*40C= ENSP00000476619.1:n.*40C=
ENST00000474458.5:c.*40C= ENSP00000476988.1:n.*40C=
ENST00000475477.5:c.*129C= ENSP00000476854.1:n.*129C=
NM_000778.3:c.1335C= NP_000769.2:p.His445=
XM_005270539.1:c.1041C= XP_005270596.1:p.His347=
XM_011540826.1:c.1353C= XP_011539128.1:p.His451=
XM_011540827.1:c.1059C= XP_011539129.1:p.His353=
XM_011540828.1:c.1041C= XP_011539130.1:p.His347=
XR_246241.1:n.1239C=
XR_246242.1:n.1223C=
NM_001319155.1:c.1239C= NP_001306084.1:p.His413=
NM_001363587.1:c.1041C= NP_001350516.1:p.His347=
NR_134988.1:n.1040C=
NR_134989.1:n.1231C=
NR_134990.1:n.1225C=
NR_134991.1:n.1212C=
NR_134992.1:n.841C=
NR_134993.1:n.975C=
NR_134994.1:n.1247C=
XM_017000465.1:c.1023C= XP_016855954.1:p.His341=
XR_001737005.1:n.1313C=
NM_000778.4:c.1335C= MANE Select NP_000769.2:p.His445=
NM_001319155.2:c.1239C= NP_001306084.1:p.His413=
NM_001363587.2:c.1041C= NP_001350516.1:p.His347=
NR_134988.2:n.1032C=
NR_134989.2:n.1223C=
NR_134990.2:n.1217C=
NR_134991.2:n.1204C=
NR_134992.2:n.833C=
NR_134993.2:n.967C=
NR_134994.2:n.1239C=