Canonical Allele Identifier: CA340223103
Gene: CYP4A11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46932765A>T , CM000663.2:g.46932765A>T GRCh38
NC_000001.10:g.47398437A>T , CM000663.1:g.47398437A>T GRCh37
NC_000001.9:g.47171024A>T NCBI36
NG_007932.1:g.13720T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000310638.9:c.1360T>A MANE Select ENSP00000311095.4:p.Ser454Thr
ENST00000310638.8:c.1360T>A ENSP00000311095.4:p.Ser454Thr
ENST00000371904.8:c.1363T>A ENSP00000360971.4:p.Ser455Thr
ENST00000371905.1:c.1360T>A ENSP00000360972.1:p.Ser454Thr
ENST00000462347.5:c.1066T>A ENSP00000477495.1:p.Ser356Thr
ENST00000465874.5:c.*158T>A ENSP00000476368.1:n.*158T>A
ENST00000468629.5:c.*65T>A ENSP00000476619.1:n.*65T>A
ENST00000474458.5:c.*65T>A ENSP00000476988.1:n.*65T>A
ENST00000475477.5:c.*154T>A ENSP00000476854.1:n.*154T>A
NM_000778.3:c.1360T>A NP_000769.2:p.Ser454Thr
XM_005270539.1:c.1066T>A XP_005270596.1:p.Ser356Thr
XM_011540826.1:c.1378T>A XP_011539128.1:p.Ser460Thr
XM_011540827.1:c.1084T>A XP_011539129.1:p.Ser362Thr
XM_011540828.1:c.1066T>A XP_011539130.1:p.Ser356Thr
XR_246241.1:n.1264T>A
XR_246242.1:n.1248T>A
NM_001319155.1:c.1264T>A NP_001306084.1:p.Ser422Thr
NM_001363587.1:c.1066T>A NP_001350516.1:p.Ser356Thr
NR_134988.1:n.1065T>A
NR_134989.1:n.1256T>A
NR_134990.1:n.1250T>A
NR_134991.1:n.1237T>A
NR_134992.1:n.866T>A
NR_134993.1:n.1000T>A
NR_134994.1:n.1272T>A
XM_017000465.1:c.1048T>A XP_016855954.1:p.Ser350Thr
XR_001737005.1:n.1338T>A
NM_000778.4:c.1360T>A MANE Select NP_000769.2:p.Ser454Thr
NM_001319155.2:c.1264T>A NP_001306084.1:p.Ser422Thr
NM_001363587.2:c.1066T>A NP_001350516.1:p.Ser356Thr
NR_134988.2:n.1057T>A
NR_134989.2:n.1248T>A
NR_134990.2:n.1242T>A
NR_134991.2:n.1229T>A
NR_134992.2:n.858T>A
NR_134993.2:n.992T>A
NR_134994.2:n.1264T>A