Canonical Allele Identifier: CA2645486284
Gene: CYP4A11 HGNC NCBI

Linked Data

gnomAD v4: 1-46933058-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46933058G>T , CM000663.2:g.46933058G>T GRCh38
NC_000001.10:g.47398730G>T , CM000663.1:g.47398730G>T GRCh37
NC_000001.9:g.47171317G>T NCBI36
NG_007932.1:g.13427C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000310638.9:c.1223-11C>A MANE Select ENSP00000311095.4:n.1223-11C>A
ENST00000310638.8:c.1223-11C>A ENSP00000311095.4:n.1223-11C>A
ENST00000371904.8:c.1226-11C>A ENSP00000360971.4:n.1226-11C>A
ENST00000371905.1:c.1223-11C>A ENSP00000360972.1:n.1223-11C>A
ENST00000462347.5:c.929-11C>A ENSP00000477495.1:n.929-11C>A
ENST00000465874.5:c.*21-11C>A ENSP00000476368.1:n.*21-11C>A
ENST00000468629.5:c.1127-221C>A ENSP00000476619.1:n.1127-221C>A
ENST00000474458.5:c.743-221C>A ENSP00000476988.1:n.743-221C>A
ENST00000475477.5:c.*82-221C>A ENSP00000476854.1:n.*82-221C>A
NM_000778.3:c.1223-11C>A NP_000769.2:n.1223-11C>A
XM_005270539.1:c.929-11C>A XP_005270596.1:n.929-11C>A
XM_011540826.1:c.1241-11C>A XP_011539128.1:n.1241-11C>A
XM_011540827.1:c.947-11C>A XP_011539129.1:n.947-11C>A
XM_011540828.1:c.929-11C>A XP_011539130.1:n.929-11C>A
XR_246241.1:n.1127-11C>A
XR_246242.1:n.1111-11C>A
NM_001319155.1:c.1127-11C>A NP_001306084.1:n.1127-11C>A
NM_001363587.1:c.929-11C>A NP_001350516.1:n.929-11C>A
NR_134988.1:n.928-11C>A
NR_134989.1:n.1119-11C>A
NR_134990.1:n.1178-221C>A
NR_134991.1:n.1100-11C>A
NR_134992.1:n.794-221C>A
NR_134993.1:n.928-221C>A
NR_134994.1:n.1135-11C>A
XM_017000465.1:c.911-11C>A XP_016855954.1:n.911-11C>A
XR_001737005.1:n.1266-221C>A
NM_000778.4:c.1223-11C>A MANE Select NP_000769.2:n.1223-11C>A
NM_001319155.2:c.1127-11C>A NP_001306084.1:n.1127-11C>A
NM_001363587.2:c.929-11C>A NP_001350516.1:n.929-11C>A
NR_134988.2:n.920-11C>A
NR_134989.2:n.1111-11C>A
NR_134990.2:n.1170-221C>A
NR_134991.2:n.1092-11C>A
NR_134992.2:n.786-221C>A
NR_134993.2:n.920-221C>A
NR_134994.2:n.1127-11C>A