Canonical Allele Identifier: CA1143930196
Gene: CYP4A11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46932812G= , CM000663.2:g.46932812G= GRCh38
NC_000001.10:g.47398484G= , CM000663.1:g.47398484G= GRCh37
NC_000001.9:g.47171071G= NCBI36
NG_007932.1:g.13673C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000310638.9:c.1313C= MANE Select ENSP00000311095.4:p.Pro438=
ENST00000310638.8:c.1313C= ENSP00000311095.4:p.Pro438=
ENST00000371904.8:c.1316C= ENSP00000360971.4:p.Pro439=
ENST00000371905.1:c.1313C= ENSP00000360972.1:p.Pro438=
ENST00000462347.5:c.1019C= ENSP00000477495.1:p.Pro340=
ENST00000465874.5:c.*111C= ENSP00000476368.1:n.*111C=
ENST00000468629.5:c.*18C= ENSP00000476619.1:n.*18C=
ENST00000474458.5:c.*18C= ENSP00000476988.1:n.*18C=
ENST00000475477.5:c.*107C= ENSP00000476854.1:n.*107C=
NM_000778.3:c.1313C= NP_000769.2:p.Pro438=
XM_005270539.1:c.1019C= XP_005270596.1:p.Pro340=
XM_011540826.1:c.1331C= XP_011539128.1:p.Pro444=
XM_011540827.1:c.1037C= XP_011539129.1:p.Pro346=
XM_011540828.1:c.1019C= XP_011539130.1:p.Pro340=
XR_246241.1:n.1217C=
XR_246242.1:n.1201C=
NM_001319155.1:c.1217C= NP_001306084.1:p.Pro406=
NM_001363587.1:c.1019C= NP_001350516.1:p.Pro340=
NR_134988.1:n.1018C=
NR_134989.1:n.1209C=
NR_134990.1:n.1203C=
NR_134991.1:n.1190C=
NR_134992.1:n.819C=
NR_134993.1:n.953C=
NR_134994.1:n.1225C=
XM_017000465.1:c.1001C= XP_016855954.1:p.Pro334=
XR_001737005.1:n.1291C=
NM_000778.4:c.1313C= MANE Select NP_000769.2:p.Pro438=
NM_001319155.2:c.1217C= NP_001306084.1:p.Pro406=
NM_001363587.2:c.1019C= NP_001350516.1:p.Pro340=
NR_134988.2:n.1010C=
NR_134989.2:n.1201C=
NR_134990.2:n.1195C=
NR_134991.2:n.1182C=
NR_134992.2:n.811C=
NR_134993.2:n.945C=
NR_134994.2:n.1217C=