Canonical Allele Identifier: CA522613157
Gene: CYP4A11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46932733A>G , CM000663.2:g.46932733A>G GRCh38
NC_000001.10:g.47398405A>G , CM000663.1:g.47398405A>G GRCh37
NC_000001.9:g.47170992A>G NCBI36
NG_007932.1:g.13752T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000310638.9:c.1364+28T>C MANE Select ENSP00000311095.4:n.1364+28T>C
ENST00000310638.8:c.1364+28T>C ENSP00000311095.4:n.1364+28T>C
ENST00000371904.8:c.1367+28T>C ENSP00000360971.4:n.1367+28T>C
ENST00000371905.1:c.*24T>C ENSP00000360972.1:n.*24T>C
ENST00000462347.5:c.1070+28T>C ENSP00000477495.1:n.1070+28T>C
ENST00000465874.5:c.*190T>C ENSP00000476368.1:n.*190T>C
ENST00000468629.5:c.*69+28T>C ENSP00000476619.1:n.*69+28T>C
ENST00000474458.5:c.*69+28T>C ENSP00000476988.1:n.*69+28T>C
ENST00000475477.5:c.*158+28T>C ENSP00000476854.1:n.*158+28T>C
NM_000778.3:c.1364+28T>C NP_000769.2:n.1364+28T>C
XM_011540826.1:c.1382+28T>C XP_011539128.1:n.1382+28T>C
XM_011540827.1:c.1088+28T>C XP_011539129.1:n.1088+28T>C
XM_011540828.1:c.1070+28T>C XP_011539130.1:n.1070+28T>C
XR_246241.1:n.1268+28T>C
XR_246242.1:n.1252+28T>C
NM_001319155.1:c.1268+28T>C NP_001306084.1:n.1268+28T>C
NM_001363587.1:c.1070+28T>C NP_001350516.1:n.1070+28T>C
NR_134988.1:n.1069+28T>C
NR_134989.1:n.1260+28T>C
NR_134990.1:n.1254+28T>C
NR_134991.1:n.1241+28T>C
NR_134992.1:n.870+28T>C
NR_134993.1:n.1004+28T>C
NR_134994.1:n.1276+28T>C
XM_017000465.1:c.1052+28T>C XP_016855954.1:n.1052+28T>C
XR_001737005.1:n.1342+28T>C
NM_000778.4:c.1364+28T>C MANE Select NP_000769.2:n.1364+28T>C
NM_001319155.2:c.1268+28T>C NP_001306084.1:n.1268+28T>C
NM_001363587.2:c.1070+28T>C NP_001350516.1:n.1070+28T>C
NR_134988.2:n.1061+28T>C
NR_134989.2:n.1252+28T>C
NR_134990.2:n.1246+28T>C
NR_134991.2:n.1233+28T>C
NR_134992.2:n.862+28T>C
NR_134993.2:n.996+28T>C
NR_134994.2:n.1268+28T>C