Canonical Allele Identifier: CA2474390699

Gene: CYP4A11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932996C= , CM000663.2:g.46932996C=	GRCh38
NC_000001.10:g.47398668C= , CM000663.1:g.47398668C=	GRCh37
NC_000001.9:g.47171255C=	NCBI36
NG_007932.1:g.13489G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1274G= MANE Select	ENSP00000311095.4:p.Trp425=
ENST00000310638.8:c.1274G=	ENSP00000311095.4:p.Trp425=
ENST00000371904.8:c.1277G=	ENSP00000360971.4:p.Trp426=
ENST00000371905.1:c.1274G=	ENSP00000360972.1:p.Trp425=
ENST00000462347.5:c.980G=	ENSP00000477495.1:p.Trp327=
ENST00000465874.5:c.*72G=	ENSP00000476368.1:n.*72G=
ENST00000468629.5:c.1127-159G=	ENSP00000476619.1:n.1127-159G=
ENST00000474458.5:c.743-159G=	ENSP00000476988.1:n.743-159G=
ENST00000475477.5:c.*82-159G=	ENSP00000476854.1:n.*82-159G=
NM_000778.3:c.1274G=	NP_000769.2:p.Trp425=
XM_005270539.1:c.980G=	XP_005270596.1:p.Trp327=
XM_011540826.1:c.1292G=	XP_011539128.1:p.Trp431=
XM_011540827.1:c.998G=	XP_011539129.1:p.Trp333=
XM_011540828.1:c.980G=	XP_011539130.1:p.Trp327=
XR_246241.1:n.1178G=
XR_246242.1:n.1162G=
NM_001319155.1:c.1178G=	NP_001306084.1:p.Trp393=
NM_001363587.1:c.980G=	NP_001350516.1:p.Trp327=
NR_134988.1:n.979G=
NR_134989.1:n.1170G=
NR_134990.1:n.1178-159G=
NR_134991.1:n.1151G=
NR_134992.1:n.794-159G=
NR_134993.1:n.928-159G=
NR_134994.1:n.1186G=
XM_017000465.1:c.962G=	XP_016855954.1:p.Trp321=
XR_001737005.1:n.1266-159G=
NM_000778.4:c.1274G= MANE Select	NP_000769.2:p.Trp425=
NM_001319155.2:c.1178G=	NP_001306084.1:p.Trp393=
NM_001363587.2:c.980G=	NP_001350516.1:p.Trp327=
NR_134988.2:n.971G=
NR_134989.2:n.1162G=
NR_134990.2:n.1170-159G=
NR_134991.2:n.1143G=
NR_134992.2:n.786-159G=
NR_134993.2:n.920-159G=
NR_134994.2:n.1178G=