Canonical Allele Identifier: CA1143367540
Gene: CYP4A11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46932821C= , CM000663.2:g.46932821C= GRCh38
NC_000001.10:g.47398493C= , CM000663.1:g.47398493C= GRCh37
NC_000001.9:g.47171080C= NCBI36
NG_007932.1:g.13664G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000310638.9:c.1304G= MANE Select ENSP00000311095.4:p.Arg435=
ENST00000310638.8:c.1304G= ENSP00000311095.4:p.Arg435=
ENST00000371904.8:c.1307G= ENSP00000360971.4:p.Arg436=
ENST00000371905.1:c.1304G= ENSP00000360972.1:p.Arg435=
ENST00000462347.5:c.1010G= ENSP00000477495.1:p.Arg337=
ENST00000465874.5:c.*102G= ENSP00000476368.1:n.*102G=
ENST00000468629.5:c.*9G= ENSP00000476619.1:n.*9G=
ENST00000474458.5:c.*9G= ENSP00000476988.1:n.*9G=
ENST00000475477.5:c.*98G= ENSP00000476854.1:n.*98G=
NM_000778.3:c.1304G= NP_000769.2:p.Arg435=
XM_005270539.1:c.1010G= XP_005270596.1:p.Arg337=
XM_011540826.1:c.1322G= XP_011539128.1:p.Arg441=
XM_011540827.1:c.1028G= XP_011539129.1:p.Arg343=
XM_011540828.1:c.1010G= XP_011539130.1:p.Arg337=
XR_246241.1:n.1208G=
XR_246242.1:n.1192G=
NM_001319155.1:c.1208G= NP_001306084.1:p.Arg403=
NM_001363587.1:c.1010G= NP_001350516.1:p.Arg337=
NR_134988.1:n.1009G=
NR_134989.1:n.1200G=
NR_134990.1:n.1194G=
NR_134991.1:n.1181G=
NR_134992.1:n.810G=
NR_134993.1:n.944G=
NR_134994.1:n.1216G=
XM_017000465.1:c.992G= XP_016855954.1:p.Arg331=
XR_001737005.1:n.1282G=
NM_000778.4:c.1304G= MANE Select NP_000769.2:p.Arg435=
NM_001319155.2:c.1208G= NP_001306084.1:p.Arg403=
NM_001363587.2:c.1010G= NP_001350516.1:p.Arg337=
NR_134988.2:n.1001G=
NR_134989.2:n.1192G=
NR_134990.2:n.1186G=
NR_134991.2:n.1173G=
NR_134992.2:n.802G=
NR_134993.2:n.936G=
NR_134994.2:n.1208G=