Canonical Allele Identifier: CA340223087
Gene: CYP4A11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46932759A>C , CM000663.2:g.46932759A>C GRCh38
NC_000001.10:g.47398431A>C , CM000663.1:g.47398431A>C GRCh37
NC_000001.9:g.47171018A>C NCBI36
NG_007932.1:g.13726T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000310638.9:c.1364+2T>G MANE Select ENSP00000311095.4:n.1364+2T>G
ENST00000310638.8:c.1364+2T>G ENSP00000311095.4:n.1364+2T>G
ENST00000371904.8:c.1367+2T>G ENSP00000360971.4:n.1367+2T>G
ENST00000371905.1:c.1366T>G ENSP00000360972.1:p.Ter456Gly
ENST00000462347.5:c.1070+2T>G ENSP00000477495.1:n.1070+2T>G
ENST00000465874.5:c.*164T>G ENSP00000476368.1:n.*164T>G
ENST00000468629.5:c.*69+2T>G ENSP00000476619.1:n.*69+2T>G
ENST00000474458.5:c.*69+2T>G ENSP00000476988.1:n.*69+2T>G
ENST00000475477.5:c.*158+2T>G ENSP00000476854.1:n.*158+2T>G
NM_000778.3:c.1364+2T>G NP_000769.2:n.1364+2T>G
XM_005270539.1:c.1072T>G XP_005270596.1:p.Ter358Gly
XM_011540826.1:c.1382+2T>G XP_011539128.1:n.1382+2T>G
XM_011540827.1:c.1088+2T>G XP_011539129.1:n.1088+2T>G
XM_011540828.1:c.1070+2T>G XP_011539130.1:n.1070+2T>G
XR_246241.1:n.1268+2T>G
XR_246242.1:n.1252+2T>G
NM_001319155.1:c.1268+2T>G NP_001306084.1:n.1268+2T>G
NM_001363587.1:c.1070+2T>G NP_001350516.1:n.1070+2T>G
NR_134988.1:n.1069+2T>G
NR_134989.1:n.1260+2T>G
NR_134990.1:n.1254+2T>G
NR_134991.1:n.1241+2T>G
NR_134992.1:n.870+2T>G
NR_134993.1:n.1004+2T>G
NR_134994.1:n.1276+2T>G
XM_017000465.1:c.1052+2T>G XP_016855954.1:n.1052+2T>G
XR_001737005.1:n.1342+2T>G
NM_000778.4:c.1364+2T>G MANE Select NP_000769.2:n.1364+2T>G
NM_001319155.2:c.1268+2T>G NP_001306084.1:n.1268+2T>G
NM_001363587.2:c.1070+2T>G NP_001350516.1:n.1070+2T>G
NR_134988.2:n.1061+2T>G
NR_134989.2:n.1252+2T>G
NR_134990.2:n.1246+2T>G
NR_134991.2:n.1233+2T>G
NR_134992.2:n.862+2T>G
NR_134993.2:n.996+2T>G
NR_134994.2:n.1268+2T>G