Canonical Allele Identifier: CA2474390532

Gene: CYP4A11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932635A= , CM000663.2:g.46932635A=	GRCh38
NC_000001.10:g.47398307A= , CM000663.1:g.47398307A=	GRCh37
NC_000001.9:g.47170894A=	NCBI36
NG_007932.1:g.13850T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000310638.9:c.1364+126T= MANE Select	ENSP00000311095.4:n.1364+126T=
ENST00000310638.8:c.1364+126T=	ENSP00000311095.4:n.1364+126T=
ENST00000371904.8:c.1367+126T=	ENSP00000360971.4:n.1367+126T=
ENST00000371905.1:c.*122T=	ENSP00000360972.1:n.*122T=
ENST00000462347.5:c.1070+126T=	ENSP00000477495.1:n.1070+126T=
ENST00000465874.5:c.*288T=	ENSP00000476368.1:n.*288T=
ENST00000468629.5:c.*69+126T=	ENSP00000476619.1:n.*69+126T=
ENST00000474458.5:c.*69+126T=	ENSP00000476988.1:n.*69+126T=
ENST00000475477.5:c.*158+126T=	ENSP00000476854.1:n.*158+126T=
NM_000778.3:c.1364+126T=	NP_000769.2:n.1364+126T=
XM_011540826.1:c.1382+126T=	XP_011539128.1:n.1382+126T=
XM_011540827.1:c.1088+126T=	XP_011539129.1:n.1088+126T=
XM_011540828.1:c.1070+126T=	XP_011539130.1:n.1070+126T=
XR_246241.1:n.1268+126T=
XR_246242.1:n.1252+126T=
NM_001319155.1:c.1268+126T=	NP_001306084.1:n.1268+126T=
NM_001363587.1:c.1070+126T=	NP_001350516.1:n.1070+126T=
NR_134988.1:n.1069+126T=
NR_134989.1:n.1260+126T=
NR_134990.1:n.1254+126T=
NR_134991.1:n.1241+126T=
NR_134992.1:n.870+126T=
NR_134993.1:n.1004+126T=
NR_134994.1:n.1276+126T=
XM_017000465.1:c.1052+126T=	XP_016855954.1:n.1052+126T=
XR_001737005.1:n.1342+126T=
NM_000778.4:c.1364+126T= MANE Select	NP_000769.2:n.1364+126T=
NM_001319155.2:c.1268+126T=	NP_001306084.1:n.1268+126T=
NM_001363587.2:c.1070+126T=	NP_001350516.1:n.1070+126T=
NR_134988.2:n.1061+126T=
NR_134989.2:n.1252+126T=
NR_134990.2:n.1246+126T=
NR_134991.2:n.1233+126T=
NR_134992.2:n.862+126T=
NR_134993.2:n.996+126T=
NR_134994.2:n.1268+126T=