Canonical Allele Identifier: CA2474390695
Gene: CYP4A11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46932989G= , CM000663.2:g.46932989G= GRCh38
NC_000001.10:g.47398661G= , CM000663.1:g.47398661G= GRCh37
NC_000001.9:g.47171248G= NCBI36
NG_007932.1:g.13496C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000310638.9:c.1281C= MANE Select ENSP00000311095.4:p.Asn427=
ENST00000310638.8:c.1281C= ENSP00000311095.4:p.Asn427=
ENST00000371904.8:c.1284C= ENSP00000360971.4:p.Asn428=
ENST00000371905.1:c.1281C= ENSP00000360972.1:p.Asn427=
ENST00000462347.5:c.987C= ENSP00000477495.1:p.Asn329=
ENST00000465874.5:c.*79C= ENSP00000476368.1:n.*79C=
ENST00000468629.5:c.1127-152C= ENSP00000476619.1:n.1127-152C=
ENST00000474458.5:c.743-152C= ENSP00000476988.1:n.743-152C=
ENST00000475477.5:c.*82-152C= ENSP00000476854.1:n.*82-152C=
NM_000778.3:c.1281C= NP_000769.2:p.Asn427=
XM_005270539.1:c.987C= XP_005270596.1:p.Asn329=
XM_011540826.1:c.1299C= XP_011539128.1:p.Asn433=
XM_011540827.1:c.1005C= XP_011539129.1:p.Asn335=
XM_011540828.1:c.987C= XP_011539130.1:p.Asn329=
XR_246241.1:n.1185C=
XR_246242.1:n.1169C=
NM_001319155.1:c.1185C= NP_001306084.1:p.Asn395=
NM_001363587.1:c.987C= NP_001350516.1:p.Asn329=
NR_134988.1:n.986C=
NR_134989.1:n.1177C=
NR_134990.1:n.1178-152C=
NR_134991.1:n.1158C=
NR_134992.1:n.794-152C=
NR_134993.1:n.928-152C=
NR_134994.1:n.1193C=
XM_017000465.1:c.969C= XP_016855954.1:p.Asn323=
XR_001737005.1:n.1266-152C=
NM_000778.4:c.1281C= MANE Select NP_000769.2:p.Asn427=
NM_001319155.2:c.1185C= NP_001306084.1:p.Asn395=
NM_001363587.2:c.987C= NP_001350516.1:p.Asn329=
NR_134988.2:n.978C=
NR_134989.2:n.1169C=
NR_134990.2:n.1170-152C=
NR_134991.2:n.1150C=
NR_134992.2:n.786-152C=
NR_134993.2:n.920-152C=
NR_134994.2:n.1185C=