Canonical Allele Identifier: CA2474390615

Gene: CYP4A11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932836A= , CM000663.2:g.46932836A=	GRCh38
NC_000001.10:g.47398508A= , CM000663.1:g.47398508A=	GRCh37
NC_000001.9:g.47171095A=	NCBI36
NG_007932.1:g.13649T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000310638.9:c.1289T= MANE Select	ENSP00000311095.4:p.Val430=
ENST00000310638.8:c.1289T=	ENSP00000311095.4:p.Val430=
ENST00000371904.8:c.1292T=	ENSP00000360971.4:p.Val431=
ENST00000371905.1:c.1289T=	ENSP00000360972.1:p.Val430=
ENST00000462347.5:c.995T=	ENSP00000477495.1:p.Val332=
ENST00000465874.5:c.*87T=	ENSP00000476368.1:n.*87T=
ENST00000468629.5:c.1128T=	ENSP00000476619.1:p.Gly376=
ENST00000474458.5:c.744T=	ENSP00000476988.1:p.Ser248=
ENST00000475477.5:c.*83T=	ENSP00000476854.1:n.*83T=
NM_000778.3:c.1289T=	NP_000769.2:p.Val430=
XM_005270539.1:c.995T=	XP_005270596.1:p.Val332=
XM_011540826.1:c.1307T=	XP_011539128.1:p.Val436=
XM_011540827.1:c.1013T=	XP_011539129.1:p.Val338=
XM_011540828.1:c.995T=	XP_011539130.1:p.Val332=
XR_246241.1:n.1193T=
XR_246242.1:n.1177T=
NM_001319155.1:c.1193T=	NP_001306084.1:p.Val398=
NM_001363587.1:c.995T=	NP_001350516.1:p.Val332=
NR_134988.1:n.994T=
NR_134989.1:n.1185T=
NR_134990.1:n.1179T=
NR_134991.1:n.1166T=
NR_134992.1:n.795T=
NR_134993.1:n.929T=
NR_134994.1:n.1201T=
XM_017000465.1:c.977T=	XP_016855954.1:p.Val326=
XR_001737005.1:n.1267T=
NM_000778.4:c.1289T= MANE Select	NP_000769.2:p.Val430=
NM_001319155.2:c.1193T=	NP_001306084.1:p.Val398=
NM_001363587.2:c.995T=	NP_001350516.1:p.Val332=
NR_134988.2:n.986T=
NR_134989.2:n.1177T=
NR_134990.2:n.1171T=
NR_134991.2:n.1158T=
NR_134992.2:n.787T=
NR_134993.2:n.921T=
NR_134994.2:n.1193T=