Canonical Allele Identifier: CA417755916
Gene: CYP4A11 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.47398504A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46932832A>G , CM000663.2:g.46932832A>G GRCh38
NC_000001.10:g.47398504A>G , CM000663.1:g.47398504A>G GRCh37
NC_000001.9:g.47171091A>G NCBI36
NG_007932.1:g.13653T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000310638.9:c.1293T>C MANE Select ENSP00000311095.4:p.Phe431=
ENST00000310638.8:c.1293T>C ENSP00000311095.4:p.Phe431=
ENST00000371904.8:c.1296T>C ENSP00000360971.4:p.Phe432=
ENST00000371905.1:c.1293T>C ENSP00000360972.1:p.Phe431=
ENST00000462347.5:c.999T>C ENSP00000477495.1:p.Phe333=
ENST00000465874.5:c.*91T>C ENSP00000476368.1:n.*91T>C
ENST00000468629.5:c.1132T>C ENSP00000476619.1:p.Ter378Arg
ENST00000474458.5:c.748T>C ENSP00000476988.1:p.Ter250Arg
ENST00000475477.5:c.*87T>C ENSP00000476854.1:n.*87T>C
NM_000778.3:c.1293T>C NP_000769.2:p.Phe431=
XM_005270539.1:c.999T>C XP_005270596.1:p.Phe333=
XM_011540826.1:c.1311T>C XP_011539128.1:p.Phe437=
XM_011540827.1:c.1017T>C XP_011539129.1:p.Phe339=
XM_011540828.1:c.999T>C XP_011539130.1:p.Phe333=
XR_246241.1:n.1197T>C
XR_246242.1:n.1181T>C
NM_001319155.1:c.1197T>C NP_001306084.1:p.Phe399=
NM_001363587.1:c.999T>C NP_001350516.1:p.Phe333=
NR_134988.1:n.998T>C
NR_134989.1:n.1189T>C
NR_134990.1:n.1183T>C
NR_134991.1:n.1170T>C
NR_134992.1:n.799T>C
NR_134993.1:n.933T>C
NR_134994.1:n.1205T>C
XM_017000465.1:c.981T>C XP_016855954.1:p.Phe327=
XR_001737005.1:n.1271T>C
NM_000778.4:c.1293T>C MANE Select NP_000769.2:p.Phe431=
NM_001319155.2:c.1197T>C NP_001306084.1:p.Phe399=
NM_001363587.2:c.999T>C NP_001350516.1:p.Phe333=
NR_134988.2:n.990T>C
NR_134989.2:n.1181T>C
NR_134990.2:n.1175T>C
NR_134991.2:n.1162T>C
NR_134992.2:n.791T>C
NR_134993.2:n.925T>C
NR_134994.2:n.1197T>C