Canonical Allele Identifier: CA340223226
Gene: CYP4A11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46932825A>C , CM000663.2:g.46932825A>C GRCh38
NC_000001.10:g.47398497A>C , CM000663.1:g.47398497A>C GRCh37
NC_000001.9:g.47171084A>C NCBI36
NG_007932.1:g.13660T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000310638.9:c.1300T>G MANE Select ENSP00000311095.4:p.Phe434Val
ENST00000310638.8:c.1300T>G ENSP00000311095.4:p.Phe434Val
ENST00000371904.8:c.1303T>G ENSP00000360971.4:p.Phe435Val
ENST00000371905.1:c.1300T>G ENSP00000360972.1:p.Phe434Val
ENST00000462347.5:c.1006T>G ENSP00000477495.1:p.Phe336Val
ENST00000465874.5:c.*98T>G ENSP00000476368.1:n.*98T>G
ENST00000468629.5:c.*5T>G ENSP00000476619.1:n.*5T>G
ENST00000474458.5:c.*5T>G ENSP00000476988.1:n.*5T>G
ENST00000475477.5:c.*94T>G ENSP00000476854.1:n.*94T>G
NM_000778.3:c.1300T>G NP_000769.2:p.Phe434Val
XM_005270539.1:c.1006T>G XP_005270596.1:p.Phe336Val
XM_011540826.1:c.1318T>G XP_011539128.1:p.Phe440Val
XM_011540827.1:c.1024T>G XP_011539129.1:p.Phe342Val
XM_011540828.1:c.1006T>G XP_011539130.1:p.Phe336Val
XR_246241.1:n.1204T>G
XR_246242.1:n.1188T>G
NM_001319155.1:c.1204T>G NP_001306084.1:p.Phe402Val
NM_001363587.1:c.1006T>G NP_001350516.1:p.Phe336Val
NR_134988.1:n.1005T>G
NR_134989.1:n.1196T>G
NR_134990.1:n.1190T>G
NR_134991.1:n.1177T>G
NR_134992.1:n.806T>G
NR_134993.1:n.940T>G
NR_134994.1:n.1212T>G
XM_017000465.1:c.988T>G XP_016855954.1:p.Phe330Val
XR_001737005.1:n.1278T>G
NM_000778.4:c.1300T>G MANE Select NP_000769.2:p.Phe434Val
NM_001319155.2:c.1204T>G NP_001306084.1:p.Phe402Val
NM_001363587.2:c.1006T>G NP_001350516.1:p.Phe336Val
NR_134988.2:n.997T>G
NR_134989.2:n.1188T>G
NR_134990.2:n.1182T>G
NR_134991.2:n.1169T>G
NR_134992.2:n.798T>G
NR_134993.2:n.932T>G
NR_134994.2:n.1204T>G