Canonical Allele Identifier: CA2474390587

Gene: CYP4A11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932762T= , CM000663.2:g.46932762T=	GRCh38
NC_000001.10:g.47398434T= , CM000663.1:g.47398434T=	GRCh37
NC_000001.9:g.47171021T=	NCBI36
NG_007932.1:g.13723A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000310638.9:c.1363A= MANE Select	ENSP00000311095.4:p.Arg455=
ENST00000310638.8:c.1363A=	ENSP00000311095.4:p.Arg455=
ENST00000371904.8:c.1366A=	ENSP00000360971.4:p.Arg456=
ENST00000371905.1:c.1363A=	ENSP00000360972.1:p.Arg455=
ENST00000462347.5:c.1069A=	ENSP00000477495.1:p.Arg357=
ENST00000465874.5:c.*161A=	ENSP00000476368.1:n.*161A=
ENST00000468629.5:c.*68A=	ENSP00000476619.1:n.*68A=
ENST00000474458.5:c.*68A=	ENSP00000476988.1:n.*68A=
ENST00000475477.5:c.*157A=	ENSP00000476854.1:n.*157A=
NM_000778.3:c.1363A=	NP_000769.2:p.Arg455=
XM_005270539.1:c.1069A=	XP_005270596.1:p.Arg357=
XM_011540826.1:c.1381A=	XP_011539128.1:p.Arg461=
XM_011540827.1:c.1087A=	XP_011539129.1:p.Arg363=
XM_011540828.1:c.1069A=	XP_011539130.1:p.Arg357=
XR_246241.1:n.1267A=
XR_246242.1:n.1251A=
NM_001319155.1:c.1267A=	NP_001306084.1:p.Arg423=
NM_001363587.1:c.1069A=	NP_001350516.1:p.Arg357=
NR_134988.1:n.1068A=
NR_134989.1:n.1259A=
NR_134990.1:n.1253A=
NR_134991.1:n.1240A=
NR_134992.1:n.869A=
NR_134993.1:n.1003A=
NR_134994.1:n.1275A=
XM_017000465.1:c.1051A=	XP_016855954.1:p.Arg351=
XR_001737005.1:n.1341A=
NM_000778.4:c.1363A= MANE Select	NP_000769.2:p.Arg455=
NM_001319155.2:c.1267A=	NP_001306084.1:p.Arg423=
NM_001363587.2:c.1069A=	NP_001350516.1:p.Arg357=
NR_134988.2:n.1060A=
NR_134989.2:n.1251A=
NR_134990.2:n.1245A=
NR_134991.2:n.1232A=
NR_134992.2:n.861A=
NR_134993.2:n.995A=
NR_134994.2:n.1267A=