Canonical Allele Identifier: CA2474390546
Gene: CYP4A11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46932669G= , CM000663.2:g.46932669G= GRCh38
NC_000001.10:g.47398341G= , CM000663.1:g.47398341G= GRCh37
NC_000001.9:g.47170928G= NCBI36
NG_007932.1:g.13816C=

Transcript Alleles

HGVS Amino-acid change
ENST00000310638.9:c.1364+92C= MANE Select ENSP00000311095.4:n.1364+92C=
ENST00000310638.8:c.1364+92C= ENSP00000311095.4:n.1364+92C=
ENST00000371904.8:c.1367+92C= ENSP00000360971.4:n.1367+92C=
ENST00000371905.1:c.*88C= ENSP00000360972.1:n.*88C=
ENST00000462347.5:c.1070+92C= ENSP00000477495.1:n.1070+92C=
ENST00000465874.5:c.*254C= ENSP00000476368.1:n.*254C=
ENST00000468629.5:c.*69+92C= ENSP00000476619.1:n.*69+92C=
ENST00000474458.5:c.*69+92C= ENSP00000476988.1:n.*69+92C=
ENST00000475477.5:c.*158+92C= ENSP00000476854.1:n.*158+92C=
NM_000778.3:c.1364+92C= NP_000769.2:n.1364+92C=
XM_011540826.1:c.1382+92C= XP_011539128.1:n.1382+92C=
XM_011540827.1:c.1088+92C= XP_011539129.1:n.1088+92C=
XM_011540828.1:c.1070+92C= XP_011539130.1:n.1070+92C=
XR_246241.1:n.1268+92C=
XR_246242.1:n.1252+92C=
NM_001319155.1:c.1268+92C= NP_001306084.1:n.1268+92C=
NM_001363587.1:c.1070+92C= NP_001350516.1:n.1070+92C=
NR_134988.1:n.1069+92C=
NR_134989.1:n.1260+92C=
NR_134990.1:n.1254+92C=
NR_134991.1:n.1241+92C=
NR_134992.1:n.870+92C=
NR_134993.1:n.1004+92C=
NR_134994.1:n.1276+92C=
XM_017000465.1:c.1052+92C= XP_016855954.1:n.1052+92C=
XR_001737005.1:n.1342+92C=
NM_000778.4:c.1364+92C= MANE Select NP_000769.2:n.1364+92C=
NM_001319155.2:c.1268+92C= NP_001306084.1:n.1268+92C=
NM_001363587.2:c.1070+92C= NP_001350516.1:n.1070+92C=
NR_134988.2:n.1061+92C=
NR_134989.2:n.1252+92C=
NR_134990.2:n.1246+92C=
NR_134991.2:n.1233+92C=
NR_134992.2:n.862+92C=
NR_134993.2:n.996+92C=
NR_134994.2:n.1268+92C=