Canonical Allele Identifier: CA2474390481

Gene: CYP4A11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932494A= , CM000663.2:g.46932494A=	GRCh38
NC_000001.10:g.47398166A= , CM000663.1:g.47398166A=	GRCh37
NC_000001.9:g.47170753A=	NCBI36
NG_007932.1:g.13991T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1364+267T= MANE Select	ENSP00000311095.4:n.1364+267T=
ENST00000310638.8:c.1364+267T=	ENSP00000311095.4:n.1364+267T=
ENST00000371904.8:c.1367+267T=	ENSP00000360971.4:n.1367+267T=
ENST00000371905.1:c.*263T=	ENSP00000360972.1:n.*263T=
ENST00000462347.5:c.1070+267T=	ENSP00000477495.1:n.1070+267T=
ENST00000465874.5:c.*429T=	ENSP00000476368.1:n.*429T=
ENST00000468629.5:c.*69+267T=	ENSP00000476619.1:n.*69+267T=
ENST00000474458.5:c.*69+267T=	ENSP00000476988.1:n.*69+267T=
ENST00000475477.5:c.*158+267T=	ENSP00000476854.1:n.*158+267T=
NM_000778.3:c.1364+267T=	NP_000769.2:n.1364+267T=
XM_011540826.1:c.1382+267T=	XP_011539128.1:n.1382+267T=
XM_011540827.1:c.1088+267T=	XP_011539129.1:n.1088+267T=
XM_011540828.1:c.1070+267T=	XP_011539130.1:n.1070+267T=
XR_246241.1:n.1268+267T=
XR_246242.1:n.1252+267T=
NM_001319155.1:c.1268+267T=	NP_001306084.1:n.1268+267T=
NM_001363587.1:c.1070+267T=	NP_001350516.1:n.1070+267T=
NR_134988.1:n.1069+267T=
NR_134989.1:n.1260+267T=
NR_134990.1:n.1254+267T=
NR_134991.1:n.1241+267T=
NR_134992.1:n.870+267T=
NR_134993.1:n.1004+267T=
NR_134994.1:n.1276+267T=
XM_017000465.1:c.1052+267T=	XP_016855954.1:n.1052+267T=
XR_001737005.1:n.1342+267T=
NM_000778.4:c.1364+267T= MANE Select	NP_000769.2:n.1364+267T=
NM_001319155.2:c.1268+267T=	NP_001306084.1:n.1268+267T=
NM_001363587.2:c.1070+267T=	NP_001350516.1:n.1070+267T=
NR_134988.2:n.1061+267T=
NR_134989.2:n.1252+267T=
NR_134990.2:n.1246+267T=
NR_134991.2:n.1233+267T=
NR_134992.2:n.862+267T=
NR_134993.2:n.996+267T=
NR_134994.2:n.1268+267T=