Canonical Allele Identifier: CA2645485314
Gene: CYP4A11 HGNC NCBI

Linked Data

gnomAD v4: 1-46931394-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46931394G>T , CM000663.2:g.46931394G>T GRCh38
NC_000001.10:g.47397066G>T , CM000663.1:g.47397066G>T GRCh37
NC_000001.9:g.47169653G>T NCBI36
NG_007932.1:g.15091C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000310638.9:c.1365-1084C>A MANE Select ENSP00000311095.4:n.1365-1084C>A
ENST00000310638.8:c.1365-1084C>A ENSP00000311095.4:n.1365-1084C>A
ENST00000371904.8:c.1368-1084C>A ENSP00000360971.4:n.1368-1084C>A
ENST00000462347.5:c.1071-1084C>A ENSP00000477495.1:n.1071-1084C>A
ENST00000468629.5:c.*70-1084C>A ENSP00000476619.1:n.*70-1084C>A
ENST00000474458.5:c.*70-1084C>A ENSP00000476988.1:n.*70-1084C>A
ENST00000475477.5:c.*159-1084C>A ENSP00000476854.1:n.*159-1084C>A
NM_000778.3:c.1365-1084C>A NP_000769.2:n.1365-1084C>A
XM_011540826.1:c.1383-1084C>A XP_011539128.1:n.1383-1084C>A
XM_011540827.1:c.1089-1084C>A XP_011539129.1:n.1089-1084C>A
XM_011540828.1:c.1071-1084C>A XP_011539130.1:n.1071-1084C>A
XR_246241.1:n.1269-1084C>A
XR_246242.1:n.1253-1084C>A
NM_001319155.1:c.1269-1084C>A NP_001306084.1:n.1269-1084C>A
NM_001363587.1:c.1071-1084C>A NP_001350516.1:n.1071-1084C>A
NR_134988.1:n.1070-1084C>A
NR_134989.1:n.1261-1084C>A
NR_134990.1:n.1255-1084C>A
NR_134991.1:n.1242-1084C>A
NR_134992.1:n.871-1084C>A
NR_134993.1:n.1005-1084C>A
NR_134994.1:n.1277-1084C>A
XM_017000465.1:c.1053-1084C>A XP_016855954.1:n.1053-1084C>A
XR_001737005.1:n.1343-1084C>A
NM_000778.4:c.1365-1084C>A MANE Select NP_000769.2:n.1365-1084C>A
NM_001319155.2:c.1269-1084C>A NP_001306084.1:n.1269-1084C>A
NM_001363587.2:c.1071-1084C>A NP_001350516.1:n.1071-1084C>A
NR_134988.2:n.1062-1084C>A
NR_134989.2:n.1253-1084C>A
NR_134990.2:n.1247-1084C>A
NR_134991.2:n.1234-1084C>A
NR_134992.2:n.863-1084C>A
NR_134993.2:n.997-1084C>A
NR_134994.2:n.1269-1084C>A