Canonical Allele Identifier: CA736355078
Gene: CYP4A11 HGNC NCBI

Linked Data

dbSNP Id: rs1157470837
gnomAD v3: 1-46932701-G-C
gnomAD v4: 1-46932701-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46932701G>C , CM000663.2:g.46932701G>C GRCh38
NC_000001.10:g.47398373G>C , CM000663.1:g.47398373G>C GRCh37
NC_000001.9:g.47170960G>C NCBI36
NG_007932.1:g.13784C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000310638.9:c.1364+60C>G MANE Select ENSP00000311095.4:n.1364+60C>G
ENST00000310638.8:c.1364+60C>G ENSP00000311095.4:n.1364+60C>G
ENST00000371904.8:c.1367+60C>G ENSP00000360971.4:n.1367+60C>G
ENST00000371905.1:c.*56C>G ENSP00000360972.1:n.*56C>G
ENST00000462347.5:c.1070+60C>G ENSP00000477495.1:n.1070+60C>G
ENST00000465874.5:c.*222C>G ENSP00000476368.1:n.*222C>G
ENST00000468629.5:c.*69+60C>G ENSP00000476619.1:n.*69+60C>G
ENST00000474458.5:c.*69+60C>G ENSP00000476988.1:n.*69+60C>G
ENST00000475477.5:c.*158+60C>G ENSP00000476854.1:n.*158+60C>G
NM_000778.3:c.1364+60C>G NP_000769.2:n.1364+60C>G
XM_011540826.1:c.1382+60C>G XP_011539128.1:n.1382+60C>G
XM_011540827.1:c.1088+60C>G XP_011539129.1:n.1088+60C>G
XM_011540828.1:c.1070+60C>G XP_011539130.1:n.1070+60C>G
XR_246241.1:n.1268+60C>G
XR_246242.1:n.1252+60C>G
NM_001319155.1:c.1268+60C>G NP_001306084.1:n.1268+60C>G
NM_001363587.1:c.1070+60C>G NP_001350516.1:n.1070+60C>G
NR_134988.1:n.1069+60C>G
NR_134989.1:n.1260+60C>G
NR_134990.1:n.1254+60C>G
NR_134991.1:n.1241+60C>G
NR_134992.1:n.870+60C>G
NR_134993.1:n.1004+60C>G
NR_134994.1:n.1276+60C>G
XM_017000465.1:c.1052+60C>G XP_016855954.1:n.1052+60C>G
XR_001737005.1:n.1342+60C>G
NM_000778.4:c.1364+60C>G MANE Select NP_000769.2:n.1364+60C>G
NM_001319155.2:c.1268+60C>G NP_001306084.1:n.1268+60C>G
NM_001363587.2:c.1070+60C>G NP_001350516.1:n.1070+60C>G
NR_134988.2:n.1061+60C>G
NR_134989.2:n.1252+60C>G
NR_134990.2:n.1246+60C>G
NR_134991.2:n.1233+60C>G
NR_134992.2:n.862+60C>G
NR_134993.2:n.996+60C>G
NR_134994.2:n.1268+60C>G