Canonical Allele Identifier: CA1148417015
Gene: CYP4A11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46932979A= , CM000663.2:g.46932979A= GRCh38
NC_000001.10:g.47398651A= , CM000663.1:g.47398651A= GRCh37
NC_000001.9:g.47171238A= NCBI36
NG_007932.1:g.13506T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000310638.9:c.1287+4T= MANE Select ENSP00000311095.4:n.1287+4T=
ENST00000310638.8:c.1287+4T= ENSP00000311095.4:n.1287+4T=
ENST00000371904.8:c.1290+4T= ENSP00000360971.4:n.1290+4T=
ENST00000371905.1:c.1287+4T= ENSP00000360972.1:n.1287+4T=
ENST00000462347.5:c.993+4T= ENSP00000477495.1:n.993+4T=
ENST00000465874.5:c.*85+4T= ENSP00000476368.1:n.*85+4T=
ENST00000468629.5:c.1127-142T= ENSP00000476619.1:n.1127-142T=
ENST00000474458.5:c.743-142T= ENSP00000476988.1:n.743-142T=
ENST00000475477.5:c.*82-142T= ENSP00000476854.1:n.*82-142T=
NM_000778.3:c.1287+4T= NP_000769.2:n.1287+4T=
XM_005270539.1:c.993+4T= XP_005270596.1:n.993+4T=
XM_011540826.1:c.1305+4T= XP_011539128.1:n.1305+4T=
XM_011540827.1:c.1011+4T= XP_011539129.1:n.1011+4T=
XM_011540828.1:c.993+4T= XP_011539130.1:n.993+4T=
XR_246241.1:n.1191+4T=
XR_246242.1:n.1175+4T=
NM_001319155.1:c.1191+4T= NP_001306084.1:n.1191+4T=
NM_001363587.1:c.993+4T= NP_001350516.1:n.993+4T=
NR_134988.1:n.992+4T=
NR_134989.1:n.1183+4T=
NR_134990.1:n.1178-142T=
NR_134991.1:n.1164+4T=
NR_134992.1:n.794-142T=
NR_134993.1:n.928-142T=
NR_134994.1:n.1199+4T=
XM_017000465.1:c.975+4T= XP_016855954.1:n.975+4T=
XR_001737005.1:n.1266-142T=
NM_000778.4:c.1287+4T= MANE Select NP_000769.2:n.1287+4T=
NM_001319155.2:c.1191+4T= NP_001306084.1:n.1191+4T=
NM_001363587.2:c.993+4T= NP_001350516.1:n.993+4T=
NR_134988.2:n.984+4T=
NR_134989.2:n.1175+4T=
NR_134990.2:n.1170-142T=
NR_134991.2:n.1156+4T=
NR_134992.2:n.786-142T=
NR_134993.2:n.920-142T=
NR_134994.2:n.1191+4T=