Canonical Allele Identifier: CA340223227
Gene: CYP4A11 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000310638.9:c.1298C>A MANE Select ENSP00000311095.4:p.Pro433His
ENST00000310638.8:c.1298C>A ENSP00000311095.4:p.Pro433His
ENST00000371904.8:c.1301C>A ENSP00000360971.4:p.Pro434His
ENST00000371905.1:c.1298C>A ENSP00000360972.1:p.Pro433His
ENST00000462347.5:c.1004C>A ENSP00000477495.1:p.Pro335His
ENST00000465874.5:c.*96C>A ENSP00000476368.1:n.*96C>A
ENST00000468629.5:c.*3C>A ENSP00000476619.1:n.*3C>A
ENST00000474458.5:c.*3C>A ENSP00000476988.1:n.*3C>A
ENST00000475477.5:c.*92C>A ENSP00000476854.1:n.*92C>A
NM_000778.3:c.1298C>A NP_000769.2:p.Pro433His
XM_005270539.1:c.1004C>A XP_005270596.1:p.Pro335His
XM_011540826.1:c.1316C>A XP_011539128.1:p.Pro439His
XM_011540827.1:c.1022C>A XP_011539129.1:p.Pro341His
XM_011540828.1:c.1004C>A XP_011539130.1:p.Pro335His
XR_246241.1:n.1202C>A
XR_246242.1:n.1186C>A
NM_001319155.1:c.1202C>A NP_001306084.1:p.Pro401His
NM_001363587.1:c.1004C>A NP_001350516.1:p.Pro335His
NR_134988.1:n.1003C>A
NR_134989.1:n.1194C>A
NR_134990.1:n.1188C>A
NR_134991.1:n.1175C>A
NR_134992.1:n.804C>A
NR_134993.1:n.938C>A
NR_134994.1:n.1210C>A
XM_017000465.1:c.986C>A XP_016855954.1:p.Pro329His
XR_001737005.1:n.1276C>A
NM_000778.4:c.1298C>A MANE Select NP_000769.2:p.Pro433His
NM_001319155.2:c.1202C>A NP_001306084.1:p.Pro401His
NM_001363587.2:c.1004C>A NP_001350516.1:p.Pro335His
NR_134988.2:n.995C>A
NR_134989.2:n.1186C>A
NR_134990.2:n.1180C>A
NR_134991.2:n.1167C>A
NR_134992.2:n.796C>A
NR_134993.2:n.930C>A
NR_134994.2:n.1202C>A