Canonical Allele Identifier: CA2474390602

Gene: CYP4A11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932801G= , CM000663.2:g.46932801G=	GRCh38
NC_000001.10:g.47398473G= , CM000663.1:g.47398473G=	GRCh37
NC_000001.9:g.47171060G=	NCBI36
NG_007932.1:g.13684C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1324C= MANE Select	ENSP00000311095.4:p.Gln442=
ENST00000310638.8:c.1324C=	ENSP00000311095.4:p.Gln442=
ENST00000371904.8:c.1327C=	ENSP00000360971.4:p.Gln443=
ENST00000371905.1:c.1324C=	ENSP00000360972.1:p.Gln442=
ENST00000462347.5:c.1030C=	ENSP00000477495.1:p.Gln344=
ENST00000465874.5:c.*122C=	ENSP00000476368.1:n.*122C=
ENST00000468629.5:c.*29C=	ENSP00000476619.1:n.*29C=
ENST00000474458.5:c.*29C=	ENSP00000476988.1:n.*29C=
ENST00000475477.5:c.*118C=	ENSP00000476854.1:n.*118C=
NM_000778.3:c.1324C=	NP_000769.2:p.Gln442=
XM_005270539.1:c.1030C=	XP_005270596.1:p.Gln344=
XM_011540826.1:c.1342C=	XP_011539128.1:p.Gln448=
XM_011540827.1:c.1048C=	XP_011539129.1:p.Gln350=
XM_011540828.1:c.1030C=	XP_011539130.1:p.Gln344=
XR_246241.1:n.1228C=
XR_246242.1:n.1212C=
NM_001319155.1:c.1228C=	NP_001306084.1:p.Gln410=
NM_001363587.1:c.1030C=	NP_001350516.1:p.Gln344=
NR_134988.1:n.1029C=
NR_134989.1:n.1220C=
NR_134990.1:n.1214C=
NR_134991.1:n.1201C=
NR_134992.1:n.830C=
NR_134993.1:n.964C=
NR_134994.1:n.1236C=
XM_017000465.1:c.1012C=	XP_016855954.1:p.Gln338=
XR_001737005.1:n.1302C=
NM_000778.4:c.1324C= MANE Select	NP_000769.2:p.Gln442=
NM_001319155.2:c.1228C=	NP_001306084.1:p.Gln410=
NM_001363587.2:c.1030C=	NP_001350516.1:p.Gln344=
NR_134988.2:n.1021C=
NR_134989.2:n.1212C=
NR_134990.2:n.1206C=
NR_134991.2:n.1193C=
NR_134992.2:n.822C=
NR_134993.2:n.956C=
NR_134994.2:n.1228C=