Canonical Allele Identifier: CA522613094
Gene: CYP4A11 HGNC NCBI

Linked Data

dbSNP Id: rs1403308556

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46932195del , CM000663.2:g.46932195del GRCh38
NC_000001.10:g.47397867del , CM000663.1:g.47397867del GRCh37
NC_000001.9:g.47170454del NCBI36
NG_007932.1:g.14290del

Transcript Alleles

HGVS Amino-acid Change
ENST00000310638.9:c.1364+566del MANE Select ENSP00000311095.4:n.1364+566del
ENST00000310638.8:c.1364+566del ENSP00000311095.4:n.1364+566del
ENST00000371904.8:c.1367+566del ENSP00000360971.4:n.1367+566del
ENST00000462347.5:c.1070+566del ENSP00000477495.1:n.1070+566del
ENST00000465874.5:c.*728del ENSP00000476368.1:n.*728del
ENST00000468629.5:c.*69+566del ENSP00000476619.1:n.*69+566del
ENST00000474458.5:c.*69+566del ENSP00000476988.1:n.*69+566del
ENST00000475477.5:c.*158+566del ENSP00000476854.1:n.*158+566del
NM_000778.3:c.1364+566del NP_000769.2:n.1364+566del
XM_011540826.1:c.1382+566del XP_011539128.1:n.1382+566del
XM_011540827.1:c.1088+566del XP_011539129.1:n.1088+566del
XM_011540828.1:c.1070+566del XP_011539130.1:n.1070+566del
XR_246241.1:n.1268+566del
XR_246242.1:n.1252+566del
NM_001319155.1:c.1268+566del NP_001306084.1:n.1268+566del
NM_001363587.1:c.1070+566del NP_001350516.1:n.1070+566del
NR_134988.1:n.1069+566del
NR_134989.1:n.1260+566del
NR_134990.1:n.1254+566del
NR_134991.1:n.1241+566del
NR_134992.1:n.870+566del
NR_134993.1:n.1004+566del
NR_134994.1:n.1276+566del
XM_017000465.1:c.1052+566del XP_016855954.1:n.1052+566del
XR_001737005.1:n.1342+566del
NM_000778.4:c.1364+566del MANE Select NP_000769.2:n.1364+566del
NM_001319155.2:c.1268+566del NP_001306084.1:n.1268+566del
NM_001363587.2:c.1070+566del NP_001350516.1:n.1070+566del
NR_134988.2:n.1061+566del
NR_134989.2:n.1252+566del
NR_134990.2:n.1246+566del
NR_134991.2:n.1233+566del
NR_134992.2:n.862+566del
NR_134993.2:n.996+566del
NR_134994.2:n.1268+566del