Canonical Allele Identifier: CA2474390847

Gene: CYP4A11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46933314A= , CM000663.2:g.46933314A=	GRCh38
NC_000001.10:g.47398986A= , CM000663.1:g.47398986A=	GRCh37
NC_000001.9:g.47171573A=	NCBI36
NG_007932.1:g.13171T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1223-267T= MANE Select	ENSP00000311095.4:n.1223-267T=
ENST00000310638.8:c.1223-267T=	ENSP00000311095.4:n.1223-267T=
ENST00000371904.8:c.1226-267T=	ENSP00000360971.4:n.1226-267T=
ENST00000371905.1:c.1223-267T=	ENSP00000360972.1:n.1223-267T=
ENST00000462347.5:c.929-267T=	ENSP00000477495.1:n.929-267T=
ENST00000465874.5:c.*21-267T=	ENSP00000476368.1:n.*21-267T=
ENST00000468629.5:c.1127-477T=	ENSP00000476619.1:n.1127-477T=
ENST00000474458.5:c.743-477T=	ENSP00000476988.1:n.743-477T=
ENST00000475477.5:c.*82-477T=	ENSP00000476854.1:n.*82-477T=
NM_000778.3:c.1223-267T=	NP_000769.2:n.1223-267T=
XM_005270539.1:c.929-267T=	XP_005270596.1:n.929-267T=
XM_011540826.1:c.1241-267T=	XP_011539128.1:n.1241-267T=
XM_011540827.1:c.947-267T=	XP_011539129.1:n.947-267T=
XM_011540828.1:c.929-267T=	XP_011539130.1:n.929-267T=
XR_246241.1:n.1127-267T=
XR_246242.1:n.1111-267T=
NM_001319155.1:c.1127-267T=	NP_001306084.1:n.1127-267T=
NM_001363587.1:c.929-267T=	NP_001350516.1:n.929-267T=
NR_134988.1:n.928-267T=
NR_134989.1:n.1119-267T=
NR_134990.1:n.1178-477T=
NR_134991.1:n.1100-267T=
NR_134992.1:n.794-477T=
NR_134993.1:n.928-477T=
NR_134994.1:n.1135-267T=
XM_017000465.1:c.911-267T=	XP_016855954.1:n.911-267T=
XR_001737005.1:n.1266-477T=
NM_000778.4:c.1223-267T= MANE Select	NP_000769.2:n.1223-267T=
NM_001319155.2:c.1127-267T=	NP_001306084.1:n.1127-267T=
NM_001363587.2:c.929-267T=	NP_001350516.1:n.929-267T=
NR_134988.2:n.920-267T=
NR_134989.2:n.1111-267T=
NR_134990.2:n.1170-477T=
NR_134991.2:n.1092-267T=
NR_134992.2:n.786-477T=
NR_134993.2:n.920-477T=
NR_134994.2:n.1127-267T=