Canonical Allele Identifier: CA340223228
Gene: CYP4A11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46932827G>A , CM000663.2:g.46932827G>A GRCh38
NC_000001.10:g.47398499G>A , CM000663.1:g.47398499G>A GRCh37
NC_000001.9:g.47171086G>A NCBI36
NG_007932.1:g.13658C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000310638.9:c.1298C>T MANE Select ENSP00000311095.4:p.Pro433Leu
ENST00000310638.8:c.1298C>T ENSP00000311095.4:p.Pro433Leu
ENST00000371904.8:c.1301C>T ENSP00000360971.4:p.Pro434Leu
ENST00000371905.1:c.1298C>T ENSP00000360972.1:p.Pro433Leu
ENST00000462347.5:c.1004C>T ENSP00000477495.1:p.Pro335Leu
ENST00000465874.5:c.*96C>T ENSP00000476368.1:n.*96C>T
ENST00000468629.5:c.*3C>T ENSP00000476619.1:n.*3C>T
ENST00000474458.5:c.*3C>T ENSP00000476988.1:n.*3C>T
ENST00000475477.5:c.*92C>T ENSP00000476854.1:n.*92C>T
NM_000778.3:c.1298C>T NP_000769.2:p.Pro433Leu
XM_005270539.1:c.1004C>T XP_005270596.1:p.Pro335Leu
XM_011540826.1:c.1316C>T XP_011539128.1:p.Pro439Leu
XM_011540827.1:c.1022C>T XP_011539129.1:p.Pro341Leu
XM_011540828.1:c.1004C>T XP_011539130.1:p.Pro335Leu
XR_246241.1:n.1202C>T
XR_246242.1:n.1186C>T
NM_001319155.1:c.1202C>T NP_001306084.1:p.Pro401Leu
NM_001363587.1:c.1004C>T NP_001350516.1:p.Pro335Leu
NR_134988.1:n.1003C>T
NR_134989.1:n.1194C>T
NR_134990.1:n.1188C>T
NR_134991.1:n.1175C>T
NR_134992.1:n.804C>T
NR_134993.1:n.938C>T
NR_134994.1:n.1210C>T
XM_017000465.1:c.986C>T XP_016855954.1:p.Pro329Leu
XR_001737005.1:n.1276C>T
NM_000778.4:c.1298C>T MANE Select NP_000769.2:p.Pro433Leu
NM_001319155.2:c.1202C>T NP_001306084.1:p.Pro401Leu
NM_001363587.2:c.1004C>T NP_001350516.1:p.Pro335Leu
NR_134988.2:n.995C>T
NR_134989.2:n.1186C>T
NR_134990.2:n.1180C>T
NR_134991.2:n.1167C>T
NR_134992.2:n.796C>T
NR_134993.2:n.930C>T
NR_134994.2:n.1202C>T