Canonical Allele Identifier: CA2474390614

Gene: CYP4A11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932833A= , CM000663.2:g.46932833A=	GRCh38
NC_000001.10:g.47398505A= , CM000663.1:g.47398505A=	GRCh37
NC_000001.9:g.47171092A=	NCBI36
NG_007932.1:g.13652T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000310638.9:c.1292T= MANE Select	ENSP00000311095.4:p.Phe431=
ENST00000310638.8:c.1292T=	ENSP00000311095.4:p.Phe431=
ENST00000371904.8:c.1295T=	ENSP00000360971.4:p.Phe432=
ENST00000371905.1:c.1292T=	ENSP00000360972.1:p.Phe431=
ENST00000462347.5:c.998T=	ENSP00000477495.1:p.Phe333=
ENST00000465874.5:c.*90T=	ENSP00000476368.1:n.*90T=
ENST00000468629.5:c.1131T=	ENSP00000476619.1:p.Val377=
ENST00000474458.5:c.747T=	ENSP00000476988.1:p.Val249=
ENST00000475477.5:c.*86T=	ENSP00000476854.1:n.*86T=
NM_000778.3:c.1292T=	NP_000769.2:p.Phe431=
XM_005270539.1:c.998T=	XP_005270596.1:p.Phe333=
XM_011540826.1:c.1310T=	XP_011539128.1:p.Phe437=
XM_011540827.1:c.1016T=	XP_011539129.1:p.Phe339=
XM_011540828.1:c.998T=	XP_011539130.1:p.Phe333=
XR_246241.1:n.1196T=
XR_246242.1:n.1180T=
NM_001319155.1:c.1196T=	NP_001306084.1:p.Phe399=
NM_001363587.1:c.998T=	NP_001350516.1:p.Phe333=
NR_134988.1:n.997T=
NR_134989.1:n.1188T=
NR_134990.1:n.1182T=
NR_134991.1:n.1169T=
NR_134992.1:n.798T=
NR_134993.1:n.932T=
NR_134994.1:n.1204T=
XM_017000465.1:c.980T=	XP_016855954.1:p.Phe327=
XR_001737005.1:n.1270T=
NM_000778.4:c.1292T= MANE Select	NP_000769.2:p.Phe431=
NM_001319155.2:c.1196T=	NP_001306084.1:p.Phe399=
NM_001363587.2:c.998T=	NP_001350516.1:p.Phe333=
NR_134988.2:n.989T=
NR_134989.2:n.1180T=
NR_134990.2:n.1174T=
NR_134991.2:n.1161T=
NR_134992.2:n.790T=
NR_134993.2:n.924T=
NR_134994.2:n.1196T=