Canonical Allele Identifier: CA839298
Gene: CYP4A11 HGNC NCBI

Linked Data

dbSNP Id: rs764550784
gnomAD v2: 1-47398544-G-T
gnomAD v4: 1-46932872-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46932872G>T , CM000663.2:g.46932872G>T GRCh38
NC_000001.10:g.47398544G>T , CM000663.1:g.47398544G>T GRCh37
NC_000001.9:g.47171131G>T NCBI36
NG_007932.1:g.13613C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000310638.9:c.1288-35C>A MANE Select ENSP00000311095.4:n.1288-35C>A
ENST00000310638.8:c.1288-35C>A ENSP00000311095.4:n.1288-35C>A
ENST00000371904.8:c.1291-35C>A ENSP00000360971.4:n.1291-35C>A
ENST00000371905.1:c.1288-35C>A ENSP00000360972.1:n.1288-35C>A
ENST00000462347.5:c.994-35C>A ENSP00000477495.1:n.994-35C>A
ENST00000465874.5:c.*86-35C>A ENSP00000476368.1:n.*86-35C>A
ENST00000468629.5:c.1127-35C>A ENSP00000476619.1:n.1127-35C>A
ENST00000474458.5:c.743-35C>A ENSP00000476988.1:n.743-35C>A
ENST00000475477.5:c.*82-35C>A ENSP00000476854.1:n.*82-35C>A
NM_000778.3:c.1288-35C>A NP_000769.2:n.1288-35C>A
XM_005270539.1:c.994-35C>A XP_005270596.1:n.994-35C>A
XM_011540826.1:c.1306-35C>A XP_011539128.1:n.1306-35C>A
XM_011540827.1:c.1012-35C>A XP_011539129.1:n.1012-35C>A
XM_011540828.1:c.994-35C>A XP_011539130.1:n.994-35C>A
XR_246241.1:n.1192-35C>A
XR_246242.1:n.1176-35C>A
NM_001319155.1:c.1192-35C>A NP_001306084.1:n.1192-35C>A
NM_001363587.1:c.994-35C>A NP_001350516.1:n.994-35C>A
NR_134988.1:n.993-35C>A
NR_134989.1:n.1184-35C>A
NR_134990.1:n.1178-35C>A
NR_134991.1:n.1165-35C>A
NR_134992.1:n.794-35C>A
NR_134993.1:n.928-35C>A
NR_134994.1:n.1200-35C>A
XM_017000465.1:c.976-35C>A XP_016855954.1:n.976-35C>A
XR_001737005.1:n.1266-35C>A
NM_000778.4:c.1288-35C>A MANE Select NP_000769.2:n.1288-35C>A
NM_001319155.2:c.1192-35C>A NP_001306084.1:n.1192-35C>A
NM_001363587.2:c.994-35C>A NP_001350516.1:n.994-35C>A
NR_134988.2:n.985-35C>A
NR_134989.2:n.1176-35C>A
NR_134990.2:n.1170-35C>A
NR_134991.2:n.1157-35C>A
NR_134992.2:n.786-35C>A
NR_134993.2:n.920-35C>A
NR_134994.2:n.1192-35C>A