Canonical Allele Identifier: CA2474390588

Gene: CYP4A11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932765A= , CM000663.2:g.46932765A=	GRCh38
NC_000001.10:g.47398437A= , CM000663.1:g.47398437A=	GRCh37
NC_000001.9:g.47171024A=	NCBI36
NG_007932.1:g.13720T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000310638.9:c.1360T= MANE Select	ENSP00000311095.4:p.Ser454=
ENST00000310638.8:c.1360T=	ENSP00000311095.4:p.Ser454=
ENST00000371904.8:c.1363T=	ENSP00000360971.4:p.Ser455=
ENST00000371905.1:c.1360T=	ENSP00000360972.1:p.Ser454=
ENST00000462347.5:c.1066T=	ENSP00000477495.1:p.Ser356=
ENST00000465874.5:c.*158T=	ENSP00000476368.1:n.*158T=
ENST00000468629.5:c.*65T=	ENSP00000476619.1:n.*65T=
ENST00000474458.5:c.*65T=	ENSP00000476988.1:n.*65T=
ENST00000475477.5:c.*154T=	ENSP00000476854.1:n.*154T=
NM_000778.3:c.1360T=	NP_000769.2:p.Ser454=
XM_005270539.1:c.1066T=	XP_005270596.1:p.Ser356=
XM_011540826.1:c.1378T=	XP_011539128.1:p.Ser460=
XM_011540827.1:c.1084T=	XP_011539129.1:p.Ser362=
XM_011540828.1:c.1066T=	XP_011539130.1:p.Ser356=
XR_246241.1:n.1264T=
XR_246242.1:n.1248T=
NM_001319155.1:c.1264T=	NP_001306084.1:p.Ser422=
NM_001363587.1:c.1066T=	NP_001350516.1:p.Ser356=
NR_134988.1:n.1065T=
NR_134989.1:n.1256T=
NR_134990.1:n.1250T=
NR_134991.1:n.1237T=
NR_134992.1:n.866T=
NR_134993.1:n.1000T=
NR_134994.1:n.1272T=
XM_017000465.1:c.1048T=	XP_016855954.1:p.Ser350=
XR_001737005.1:n.1338T=
NM_000778.4:c.1360T= MANE Select	NP_000769.2:p.Ser454=
NM_001319155.2:c.1264T=	NP_001306084.1:p.Ser422=
NM_001363587.2:c.1066T=	NP_001350516.1:p.Ser356=
NR_134988.2:n.1057T=
NR_134989.2:n.1248T=
NR_134990.2:n.1242T=
NR_134991.2:n.1229T=
NR_134992.2:n.858T=
NR_134993.2:n.992T=
NR_134994.2:n.1264T=