Canonical Allele Identifier: CA2474390613

Gene: CYP4A11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932831C= , CM000663.2:g.46932831C=	GRCh38
NC_000001.10:g.47398503C= , CM000663.1:g.47398503C=	GRCh37
NC_000001.9:g.47171090C=	NCBI36
NG_007932.1:g.13654G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000310638.9:c.1294G= MANE Select	ENSP00000311095.4:p.Asp432=
ENST00000310638.8:c.1294G=	ENSP00000311095.4:p.Asp432=
ENST00000371904.8:c.1297G=	ENSP00000360971.4:p.Asp433=
ENST00000371905.1:c.1294G=	ENSP00000360972.1:p.Asp432=
ENST00000462347.5:c.1000G=	ENSP00000477495.1:p.Asp334=
ENST00000465874.5:c.*92G=	ENSP00000476368.1:n.*92G=
ENST00000468629.5:c.1133G=	ENSP00000476619.1:p.Ter378=
ENST00000474458.5:c.749G=	ENSP00000476988.1:p.Ter250=
ENST00000475477.5:c.*88G=	ENSP00000476854.1:n.*88G=
NM_000778.3:c.1294G=	NP_000769.2:p.Asp432=
XM_005270539.1:c.1000G=	XP_005270596.1:p.Asp334=
XM_011540826.1:c.1312G=	XP_011539128.1:p.Asp438=
XM_011540827.1:c.1018G=	XP_011539129.1:p.Asp340=
XM_011540828.1:c.1000G=	XP_011539130.1:p.Asp334=
XR_246241.1:n.1198G=
XR_246242.1:n.1182G=
NM_001319155.1:c.1198G=	NP_001306084.1:p.Asp400=
NM_001363587.1:c.1000G=	NP_001350516.1:p.Asp334=
NR_134988.1:n.999G=
NR_134989.1:n.1190G=
NR_134990.1:n.1184G=
NR_134991.1:n.1171G=
NR_134992.1:n.800G=
NR_134993.1:n.934G=
NR_134994.1:n.1206G=
XM_017000465.1:c.982G=	XP_016855954.1:p.Asp328=
XR_001737005.1:n.1272G=
NM_000778.4:c.1294G= MANE Select	NP_000769.2:p.Asp432=
NM_001319155.2:c.1198G=	NP_001306084.1:p.Asp400=
NM_001363587.2:c.1000G=	NP_001350516.1:p.Asp334=
NR_134988.2:n.991G=
NR_134989.2:n.1182G=
NR_134990.2:n.1176G=
NR_134991.2:n.1163G=
NR_134992.2:n.792G=
NR_134993.2:n.926G=
NR_134994.2:n.1198G=