Canonical Allele Identifier: CA1001357197
Gene: CYP4A11 HGNC NCBI

Linked Data

dbSNP Id: rs1681013333
gnomAD v3: 1-46931283-G-A
gnomAD v4: 1-46931283-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46931283G>A , CM000663.2:g.46931283G>A GRCh38
NC_000001.10:g.47396955G>A , CM000663.1:g.47396955G>A GRCh37
NC_000001.9:g.47169542G>A NCBI36
NG_007932.1:g.15202C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000310638.9:c.1365-973C>T MANE Select ENSP00000311095.4:n.1365-973C>T
ENST00000310638.8:c.1365-973C>T ENSP00000311095.4:n.1365-973C>T
ENST00000371904.8:c.1368-973C>T ENSP00000360971.4:n.1368-973C>T
ENST00000462347.5:c.1071-973C>T ENSP00000477495.1:n.1071-973C>T
ENST00000468629.5:c.*70-973C>T ENSP00000476619.1:n.*70-973C>T
ENST00000474458.5:c.*70-973C>T ENSP00000476988.1:n.*70-973C>T
ENST00000475477.5:c.*159-973C>T ENSP00000476854.1:n.*159-973C>T
NM_000778.3:c.1365-973C>T NP_000769.2:n.1365-973C>T
XM_011540826.1:c.1383-973C>T XP_011539128.1:n.1383-973C>T
XM_011540827.1:c.1089-973C>T XP_011539129.1:n.1089-973C>T
XM_011540828.1:c.1071-973C>T XP_011539130.1:n.1071-973C>T
XR_246241.1:n.1269-973C>T
XR_246242.1:n.1253-973C>T
NM_001319155.1:c.1269-973C>T NP_001306084.1:n.1269-973C>T
NM_001363587.1:c.1071-973C>T NP_001350516.1:n.1071-973C>T
NR_134988.1:n.1070-973C>T
NR_134989.1:n.1261-973C>T
NR_134990.1:n.1255-973C>T
NR_134991.1:n.1242-973C>T
NR_134992.1:n.871-973C>T
NR_134993.1:n.1005-973C>T
NR_134994.1:n.1277-973C>T
XM_017000465.1:c.1053-973C>T XP_016855954.1:n.1053-973C>T
XR_001737005.1:n.1343-973C>T
NM_000778.4:c.1365-973C>T MANE Select NP_000769.2:n.1365-973C>T
NM_001319155.2:c.1269-973C>T NP_001306084.1:n.1269-973C>T
NM_001363587.2:c.1071-973C>T NP_001350516.1:n.1071-973C>T
NR_134988.2:n.1062-973C>T
NR_134989.2:n.1253-973C>T
NR_134990.2:n.1247-973C>T
NR_134991.2:n.1234-973C>T
NR_134992.2:n.863-973C>T
NR_134993.2:n.997-973C>T
NR_134994.2:n.1269-973C>T