Canonical Allele Identifier: CA2474390708
Gene: CYP4A11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46933022A= , CM000663.2:g.46933022A= GRCh38
NC_000001.10:g.47398694A= , CM000663.1:g.47398694A= GRCh37
NC_000001.9:g.47171281A= NCBI36
NG_007932.1:g.13463T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000310638.9:c.1248T= MANE Select ENSP00000311095.4:p.Tyr416=
ENST00000310638.8:c.1248T= ENSP00000311095.4:p.Tyr416=
ENST00000371904.8:c.1251T= ENSP00000360971.4:p.Tyr417=
ENST00000371905.1:c.1248T= ENSP00000360972.1:p.Tyr416=
ENST00000462347.5:c.954T= ENSP00000477495.1:p.Tyr318=
ENST00000465874.5:c.*46T= ENSP00000476368.1:n.*46T=
ENST00000468629.5:c.1127-185T= ENSP00000476619.1:n.1127-185T=
ENST00000474458.5:c.743-185T= ENSP00000476988.1:n.743-185T=
ENST00000475477.5:c.*82-185T= ENSP00000476854.1:n.*82-185T=
NM_000778.3:c.1248T= NP_000769.2:p.Tyr416=
XM_005270539.1:c.954T= XP_005270596.1:p.Tyr318=
XM_011540826.1:c.1266T= XP_011539128.1:p.Tyr422=
XM_011540827.1:c.972T= XP_011539129.1:p.Tyr324=
XM_011540828.1:c.954T= XP_011539130.1:p.Tyr318=
XR_246241.1:n.1152T=
XR_246242.1:n.1136T=
NM_001319155.1:c.1152T= NP_001306084.1:p.Tyr384=
NM_001363587.1:c.954T= NP_001350516.1:p.Tyr318=
NR_134988.1:n.953T=
NR_134989.1:n.1144T=
NR_134990.1:n.1178-185T=
NR_134991.1:n.1125T=
NR_134992.1:n.794-185T=
NR_134993.1:n.928-185T=
NR_134994.1:n.1160T=
XM_017000465.1:c.936T= XP_016855954.1:p.Tyr312=
XR_001737005.1:n.1266-185T=
NM_000778.4:c.1248T= MANE Select NP_000769.2:p.Tyr416=
NM_001319155.2:c.1152T= NP_001306084.1:p.Tyr384=
NM_001363587.2:c.954T= NP_001350516.1:p.Tyr318=
NR_134988.2:n.945T=
NR_134989.2:n.1136T=
NR_134990.2:n.1170-185T=
NR_134991.2:n.1117T=
NR_134992.2:n.786-185T=
NR_134993.2:n.920-185T=
NR_134994.2:n.1152T=