Canonical Allele Identifier: CA340223085
Gene: CYP4A11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46932757T>G , CM000663.2:g.46932757T>G GRCh38
NC_000001.10:g.47398429T>G , CM000663.1:g.47398429T>G GRCh37
NC_000001.9:g.47171016T>G NCBI36
NG_007932.1:g.13728A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000310638.9:c.1364+4A>C MANE Select ENSP00000311095.4:n.1364+4A>C
ENST00000310638.8:c.1364+4A>C ENSP00000311095.4:n.1364+4A>C
ENST00000371904.8:c.1367+4A>C ENSP00000360971.4:n.1367+4A>C
ENST00000371905.1:c.1368A>C ENSP00000360972.1:p.Ter456Cys
ENST00000462347.5:c.1070+4A>C ENSP00000477495.1:n.1070+4A>C
ENST00000465874.5:c.*166A>C ENSP00000476368.1:n.*166A>C
ENST00000468629.5:c.*69+4A>C ENSP00000476619.1:n.*69+4A>C
ENST00000474458.5:c.*69+4A>C ENSP00000476988.1:n.*69+4A>C
ENST00000475477.5:c.*158+4A>C ENSP00000476854.1:n.*158+4A>C
NM_000778.3:c.1364+4A>C NP_000769.2:n.1364+4A>C
XM_005270539.1:c.1074A>C XP_005270596.1:p.Ter358Cys
XM_011540826.1:c.1382+4A>C XP_011539128.1:n.1382+4A>C
XM_011540827.1:c.1088+4A>C XP_011539129.1:n.1088+4A>C
XM_011540828.1:c.1070+4A>C XP_011539130.1:n.1070+4A>C
XR_246241.1:n.1268+4A>C
XR_246242.1:n.1252+4A>C
NM_001319155.1:c.1268+4A>C NP_001306084.1:n.1268+4A>C
NM_001363587.1:c.1070+4A>C NP_001350516.1:n.1070+4A>C
NR_134988.1:n.1069+4A>C
NR_134989.1:n.1260+4A>C
NR_134990.1:n.1254+4A>C
NR_134991.1:n.1241+4A>C
NR_134992.1:n.870+4A>C
NR_134993.1:n.1004+4A>C
NR_134994.1:n.1276+4A>C
XM_017000465.1:c.1052+4A>C XP_016855954.1:n.1052+4A>C
XR_001737005.1:n.1342+4A>C
NM_000778.4:c.1364+4A>C MANE Select NP_000769.2:n.1364+4A>C
NM_001319155.2:c.1268+4A>C NP_001306084.1:n.1268+4A>C
NM_001363587.2:c.1070+4A>C NP_001350516.1:n.1070+4A>C
NR_134988.2:n.1061+4A>C
NR_134989.2:n.1252+4A>C
NR_134990.2:n.1246+4A>C
NR_134991.2:n.1233+4A>C
NR_134992.2:n.862+4A>C
NR_134993.2:n.996+4A>C
NR_134994.2:n.1268+4A>C