Canonical Allele Identifier: CA2474390600
Gene: CYP4A11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46932798G= , CM000663.2:g.46932798G= GRCh38
NC_000001.10:g.47398470G= , CM000663.1:g.47398470G= GRCh37
NC_000001.9:g.47171057G= NCBI36
NG_007932.1:g.13687C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000310638.9:c.1327C= MANE Select ENSP00000311095.4:p.His443=
ENST00000310638.8:c.1327C= ENSP00000311095.4:p.His443=
ENST00000371904.8:c.1330C= ENSP00000360971.4:p.His444=
ENST00000371905.1:c.1327C= ENSP00000360972.1:p.His443=
ENST00000462347.5:c.1033C= ENSP00000477495.1:p.His345=
ENST00000465874.5:c.*125C= ENSP00000476368.1:n.*125C=
ENST00000468629.5:c.*32C= ENSP00000476619.1:n.*32C=
ENST00000474458.5:c.*32C= ENSP00000476988.1:n.*32C=
ENST00000475477.5:c.*121C= ENSP00000476854.1:n.*121C=
NM_000778.3:c.1327C= NP_000769.2:p.His443=
XM_005270539.1:c.1033C= XP_005270596.1:p.His345=
XM_011540826.1:c.1345C= XP_011539128.1:p.His449=
XM_011540827.1:c.1051C= XP_011539129.1:p.His351=
XM_011540828.1:c.1033C= XP_011539130.1:p.His345=
XR_246241.1:n.1231C=
XR_246242.1:n.1215C=
NM_001319155.1:c.1231C= NP_001306084.1:p.His411=
NM_001363587.1:c.1033C= NP_001350516.1:p.His345=
NR_134988.1:n.1032C=
NR_134989.1:n.1223C=
NR_134990.1:n.1217C=
NR_134991.1:n.1204C=
NR_134992.1:n.833C=
NR_134993.1:n.967C=
NR_134994.1:n.1239C=
XM_017000465.1:c.1015C= XP_016855954.1:p.His339=
XR_001737005.1:n.1305C=
NM_000778.4:c.1327C= MANE Select NP_000769.2:p.His443=
NM_001319155.2:c.1231C= NP_001306084.1:p.His411=
NM_001363587.2:c.1033C= NP_001350516.1:p.His345=
NR_134988.2:n.1024C=
NR_134989.2:n.1215C=
NR_134990.2:n.1209C=
NR_134991.2:n.1196C=
NR_134992.2:n.825C=
NR_134993.2:n.959C=
NR_134994.2:n.1231C=