Canonical Allele Identifier: CA2474390610
Gene: CYP4A11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46932826_46932827delinsAG , CM000663.2:g.46932826_46932827delinsAG GRCh38
NC_000001.10:g.47398498_47398499delinsAG , CM000663.1:g.47398498_47398499delinsAG GRCh37
NC_000001.9:g.47171085_47171086delinsAG NCBI36
NG_007932.1:g.13658_13659delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000310638.9:c.1298_1299delinsCT MANE Select ENSP00000311095.4:p.Pro433=
ENST00000310638.8:c.1298_1299delinsCT ENSP00000311095.4:p.Pro433=
ENST00000371904.8:c.1301_1302delinsCT ENSP00000360971.4:p.Pro434=
ENST00000371905.1:c.1298_1299delinsCT ENSP00000360972.1:p.Pro433=
ENST00000462347.5:c.1004_1005delinsCT ENSP00000477495.1:p.Pro335=
ENST00000465874.5:c.*96_*97delinsCT ENSP00000476368.1:n.*96_*97delinsCT
ENST00000468629.5:c.*3_*4delinsCT ENSP00000476619.1:n.*3_*4delinsCT
ENST00000474458.5:c.*3_*4delinsCT ENSP00000476988.1:n.*3_*4delinsCT
ENST00000475477.5:c.*92_*93delinsCT ENSP00000476854.1:n.*92_*93delinsCT
NM_000778.3:c.1298_1299delinsCT NP_000769.2:p.Pro433=
XM_005270539.1:c.1004_1005delinsCT XP_005270596.1:p.Pro335=
XM_011540826.1:c.1316_1317delinsCT XP_011539128.1:p.Pro439=
XM_011540827.1:c.1022_1023delinsCT XP_011539129.1:p.Pro341=
XM_011540828.1:c.1004_1005delinsCT XP_011539130.1:p.Pro335=
XR_246241.1:n.1202_1203delinsCT
XR_246242.1:n.1186_1187delinsCT
NM_001319155.1:c.1202_1203delinsCT NP_001306084.1:p.Pro401=
NM_001363587.1:c.1004_1005delinsCT NP_001350516.1:p.Pro335=
NR_134988.1:n.1003_1004delinsCT
NR_134989.1:n.1194_1195delinsCT
NR_134990.1:n.1188_1189delinsCT
NR_134991.1:n.1175_1176delinsCT
NR_134992.1:n.804_805delinsCT
NR_134993.1:n.938_939delinsCT
NR_134994.1:n.1210_1211delinsCT
XM_017000465.1:c.986_987delinsCT XP_016855954.1:p.Pro329=
XR_001737005.1:n.1276_1277delinsCT
NM_000778.4:c.1298_1299delinsCT MANE Select NP_000769.2:p.Pro433=
NM_001319155.2:c.1202_1203delinsCT NP_001306084.1:p.Pro401=
NM_001363587.2:c.1004_1005delinsCT NP_001350516.1:p.Pro335=
NR_134988.2:n.995_996delinsCT
NR_134989.2:n.1186_1187delinsCT
NR_134990.2:n.1180_1181delinsCT
NR_134991.2:n.1167_1168delinsCT
NR_134992.2:n.796_797delinsCT
NR_134993.2:n.930_931delinsCT
NR_134994.2:n.1202_1203delinsCT