Canonical Allele Identifier: CA10878014
Gene: CYP4A11 HGNC NCBI

Linked Data

dbSNP Id: rs9333025
gnomAD v2: 1-47396903-C-T
gnomAD v3: 1-46931231-C-T
gnomAD v4: 1-46931231-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46931231C>T , CM000663.2:g.46931231C>T GRCh38
NC_000001.10:g.47396903C>T , CM000663.1:g.47396903C>T GRCh37
NC_000001.9:g.47169490C>T NCBI36
NG_007932.1:g.15254G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000310638.9:c.1365-921G>A MANE Select ENSP00000311095.4:n.1365-921G>A
ENST00000310638.8:c.1365-921G>A ENSP00000311095.4:n.1365-921G>A
ENST00000371904.8:c.1368-921G>A ENSP00000360971.4:n.1368-921G>A
ENST00000462347.5:c.1071-921G>A ENSP00000477495.1:n.1071-921G>A
ENST00000468629.5:c.*70-921G>A ENSP00000476619.1:n.*70-921G>A
ENST00000474458.5:c.*70-921G>A ENSP00000476988.1:n.*70-921G>A
ENST00000475477.5:c.*159-921G>A ENSP00000476854.1:n.*159-921G>A
NM_000778.3:c.1365-921G>A NP_000769.2:n.1365-921G>A
XM_011540826.1:c.1383-921G>A XP_011539128.1:n.1383-921G>A
XM_011540827.1:c.1089-921G>A XP_011539129.1:n.1089-921G>A
XM_011540828.1:c.1071-921G>A XP_011539130.1:n.1071-921G>A
XR_246241.1:n.1269-921G>A
XR_246242.1:n.1253-921G>A
NM_001319155.1:c.1269-921G>A NP_001306084.1:n.1269-921G>A
NM_001363587.1:c.1071-921G>A NP_001350516.1:n.1071-921G>A
NR_134988.1:n.1070-921G>A
NR_134989.1:n.1261-921G>A
NR_134990.1:n.1255-921G>A
NR_134991.1:n.1242-921G>A
NR_134992.1:n.871-921G>A
NR_134993.1:n.1005-921G>A
NR_134994.1:n.1277-921G>A
XM_017000465.1:c.1053-921G>A XP_016855954.1:n.1053-921G>A
XR_001737005.1:n.1343-921G>A
NM_000778.4:c.1365-921G>A MANE Select NP_000769.2:n.1365-921G>A
NM_001319155.2:c.1269-921G>A NP_001306084.1:n.1269-921G>A
NM_001363587.2:c.1071-921G>A NP_001350516.1:n.1071-921G>A
NR_134988.2:n.1062-921G>A
NR_134989.2:n.1253-921G>A
NR_134990.2:n.1247-921G>A
NR_134991.2:n.1234-921G>A
NR_134992.2:n.863-921G>A
NR_134993.2:n.997-921G>A
NR_134994.2:n.1269-921G>A