Canonical Allele Identifier: CA1141648255
Gene: CYP4A11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46932827G= , CM000663.2:g.46932827G= GRCh38
NC_000001.10:g.47398499G= , CM000663.1:g.47398499G= GRCh37
NC_000001.9:g.47171086G= NCBI36
NG_007932.1:g.13658C=

Transcript Alleles

HGVS Amino-acid change
ENST00000310638.9:c.1298C= MANE Select ENSP00000311095.4:p.Pro433=
ENST00000310638.8:c.1298C= ENSP00000311095.4:p.Pro433=
ENST00000371904.8:c.1301C= ENSP00000360971.4:p.Pro434=
ENST00000371905.1:c.1298C= ENSP00000360972.1:p.Pro433=
ENST00000462347.5:c.1004C= ENSP00000477495.1:p.Pro335=
ENST00000465874.5:c.*96C= ENSP00000476368.1:n.*96C=
ENST00000468629.5:c.*3C= ENSP00000476619.1:n.*3C=
ENST00000474458.5:c.*3C= ENSP00000476988.1:n.*3C=
ENST00000475477.5:c.*92C= ENSP00000476854.1:n.*92C=
NM_000778.3:c.1298C= NP_000769.2:p.Pro433=
XM_005270539.1:c.1004C= XP_005270596.1:p.Pro335=
XM_011540826.1:c.1316C= XP_011539128.1:p.Pro439=
XM_011540827.1:c.1022C= XP_011539129.1:p.Pro341=
XM_011540828.1:c.1004C= XP_011539130.1:p.Pro335=
XR_246241.1:n.1202C=
XR_246242.1:n.1186C=
NM_001319155.1:c.1202C= NP_001306084.1:p.Pro401=
NM_001363587.1:c.1004C= NP_001350516.1:p.Pro335=
NR_134988.1:n.1003C=
NR_134989.1:n.1194C=
NR_134990.1:n.1188C=
NR_134991.1:n.1175C=
NR_134992.1:n.804C=
NR_134993.1:n.938C=
NR_134994.1:n.1210C=
XM_017000465.1:c.986C= XP_016855954.1:p.Pro329=
XR_001737005.1:n.1276C=
NM_000778.4:c.1298C= MANE Select NP_000769.2:p.Pro433=
NM_001319155.2:c.1202C= NP_001306084.1:p.Pro401=
NM_001363587.2:c.1004C= NP_001350516.1:p.Pro335=
NR_134988.2:n.995C=
NR_134989.2:n.1186C=
NR_134990.2:n.1180C=
NR_134991.2:n.1167C=
NR_134992.2:n.796C=
NR_134993.2:n.930C=
NR_134994.2:n.1202C=