Canonical Allele Identifier: CA2474390590

Gene: CYP4A11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932767C= , CM000663.2:g.46932767C=	GRCh38
NC_000001.10:g.47398439C= , CM000663.1:g.47398439C=	GRCh37
NC_000001.9:g.47171026C=	NCBI36
NG_007932.1:g.13718G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000310638.9:c.1358G= MANE Select	ENSP00000311095.4:p.Gly453=
ENST00000310638.8:c.1358G=	ENSP00000311095.4:p.Gly453=
ENST00000371904.8:c.1361G=	ENSP00000360971.4:p.Gly454=
ENST00000371905.1:c.1358G=	ENSP00000360972.1:p.Gly453=
ENST00000462347.5:c.1064G=	ENSP00000477495.1:p.Gly355=
ENST00000465874.5:c.*156G=	ENSP00000476368.1:n.*156G=
ENST00000468629.5:c.*63G=	ENSP00000476619.1:n.*63G=
ENST00000474458.5:c.*63G=	ENSP00000476988.1:n.*63G=
ENST00000475477.5:c.*152G=	ENSP00000476854.1:n.*152G=
NM_000778.3:c.1358G=	NP_000769.2:p.Gly453=
XM_005270539.1:c.1064G=	XP_005270596.1:p.Gly355=
XM_011540826.1:c.1376G=	XP_011539128.1:p.Gly459=
XM_011540827.1:c.1082G=	XP_011539129.1:p.Gly361=
XM_011540828.1:c.1064G=	XP_011539130.1:p.Gly355=
XR_246241.1:n.1262G=
XR_246242.1:n.1246G=
NM_001319155.1:c.1262G=	NP_001306084.1:p.Gly421=
NM_001363587.1:c.1064G=	NP_001350516.1:p.Gly355=
NR_134988.1:n.1063G=
NR_134989.1:n.1254G=
NR_134990.1:n.1248G=
NR_134991.1:n.1235G=
NR_134992.1:n.864G=
NR_134993.1:n.998G=
NR_134994.1:n.1270G=
XM_017000465.1:c.1046G=	XP_016855954.1:p.Gly349=
XR_001737005.1:n.1336G=
NM_000778.4:c.1358G= MANE Select	NP_000769.2:p.Gly453=
NM_001319155.2:c.1262G=	NP_001306084.1:p.Gly421=
NM_001363587.2:c.1064G=	NP_001350516.1:p.Gly355=
NR_134988.2:n.1055G=
NR_134989.2:n.1246G=
NR_134990.2:n.1240G=
NR_134991.2:n.1227G=
NR_134992.2:n.856G=
NR_134993.2:n.990G=
NR_134994.2:n.1262G=