Canonical Allele Identifier: CA340223223
Gene: CYP4A11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46932824A>T , CM000663.2:g.46932824A>T GRCh38
NC_000001.10:g.47398496A>T , CM000663.1:g.47398496A>T GRCh37
NC_000001.9:g.47171083A>T NCBI36
NG_007932.1:g.13661T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000310638.9:c.1301T>A MANE Select ENSP00000311095.4:p.Phe434Tyr
ENST00000310638.8:c.1301T>A ENSP00000311095.4:p.Phe434Tyr
ENST00000371904.8:c.1304T>A ENSP00000360971.4:p.Phe435Tyr
ENST00000371905.1:c.1301T>A ENSP00000360972.1:p.Phe434Tyr
ENST00000462347.5:c.1007T>A ENSP00000477495.1:p.Phe336Tyr
ENST00000465874.5:c.*99T>A ENSP00000476368.1:n.*99T>A
ENST00000468629.5:c.*6T>A ENSP00000476619.1:n.*6T>A
ENST00000474458.5:c.*6T>A ENSP00000476988.1:n.*6T>A
ENST00000475477.5:c.*95T>A ENSP00000476854.1:n.*95T>A
NM_000778.3:c.1301T>A NP_000769.2:p.Phe434Tyr
XM_005270539.1:c.1007T>A XP_005270596.1:p.Phe336Tyr
XM_011540826.1:c.1319T>A XP_011539128.1:p.Phe440Tyr
XM_011540827.1:c.1025T>A XP_011539129.1:p.Phe342Tyr
XM_011540828.1:c.1007T>A XP_011539130.1:p.Phe336Tyr
XR_246241.1:n.1205T>A
XR_246242.1:n.1189T>A
NM_001319155.1:c.1205T>A NP_001306084.1:p.Phe402Tyr
NM_001363587.1:c.1007T>A NP_001350516.1:p.Phe336Tyr
NR_134988.1:n.1006T>A
NR_134989.1:n.1197T>A
NR_134990.1:n.1191T>A
NR_134991.1:n.1178T>A
NR_134992.1:n.807T>A
NR_134993.1:n.941T>A
NR_134994.1:n.1213T>A
XM_017000465.1:c.989T>A XP_016855954.1:p.Phe330Tyr
XR_001737005.1:n.1279T>A
NM_000778.4:c.1301T>A MANE Select NP_000769.2:p.Phe434Tyr
NM_001319155.2:c.1205T>A NP_001306084.1:p.Phe402Tyr
NM_001363587.2:c.1007T>A NP_001350516.1:p.Phe336Tyr
NR_134988.2:n.998T>A
NR_134989.2:n.1189T>A
NR_134990.2:n.1183T>A
NR_134991.2:n.1170T>A
NR_134992.2:n.799T>A
NR_134993.2:n.933T>A
NR_134994.2:n.1205T>A