Canonical Allele Identifier: CA2474390469

Gene: CYP4A11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932438G= , CM000663.2:g.46932438G=	GRCh38
NC_000001.10:g.47398110G= , CM000663.1:g.47398110G=	GRCh37
NC_000001.9:g.47170697G=	NCBI36
NG_007932.1:g.14047C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1364+323C= MANE Select	ENSP00000311095.4:n.1364+323C=
ENST00000310638.8:c.1364+323C=	ENSP00000311095.4:n.1364+323C=
ENST00000371904.8:c.1367+323C=	ENSP00000360971.4:n.1367+323C=
ENST00000371905.1:c.*319C=	ENSP00000360972.1:n.*319C=
ENST00000462347.5:c.1070+323C=	ENSP00000477495.1:n.1070+323C=
ENST00000465874.5:c.*485C=	ENSP00000476368.1:n.*485C=
ENST00000468629.5:c.*69+323C=	ENSP00000476619.1:n.*69+323C=
ENST00000474458.5:c.*69+323C=	ENSP00000476988.1:n.*69+323C=
ENST00000475477.5:c.*158+323C=	ENSP00000476854.1:n.*158+323C=
NM_000778.3:c.1364+323C=	NP_000769.2:n.1364+323C=
XM_011540826.1:c.1382+323C=	XP_011539128.1:n.1382+323C=
XM_011540827.1:c.1088+323C=	XP_011539129.1:n.1088+323C=
XM_011540828.1:c.1070+323C=	XP_011539130.1:n.1070+323C=
XR_246241.1:n.1268+323C=
XR_246242.1:n.1252+323C=
NM_001319155.1:c.1268+323C=	NP_001306084.1:n.1268+323C=
NM_001363587.1:c.1070+323C=	NP_001350516.1:n.1070+323C=
NR_134988.1:n.1069+323C=
NR_134989.1:n.1260+323C=
NR_134990.1:n.1254+323C=
NR_134991.1:n.1241+323C=
NR_134992.1:n.870+323C=
NR_134993.1:n.1004+323C=
NR_134994.1:n.1276+323C=
XM_017000465.1:c.1052+323C=	XP_016855954.1:n.1052+323C=
XR_001737005.1:n.1342+323C=
NM_000778.4:c.1364+323C= MANE Select	NP_000769.2:n.1364+323C=
NM_001319155.2:c.1268+323C=	NP_001306084.1:n.1268+323C=
NM_001363587.2:c.1070+323C=	NP_001350516.1:n.1070+323C=
NR_134988.2:n.1061+323C=
NR_134989.2:n.1252+323C=
NR_134990.2:n.1246+323C=
NR_134991.2:n.1233+323C=
NR_134992.2:n.862+323C=
NR_134993.2:n.996+323C=
NR_134994.2:n.1268+323C=