Canonical Allele Identifier: CA2474390698

Gene: CYP4A11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932995C= , CM000663.2:g.46932995C=	GRCh38
NC_000001.10:g.47398667C= , CM000663.1:g.47398667C=	GRCh37
NC_000001.9:g.47171254C=	NCBI36
NG_007932.1:g.13490G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1275G= MANE Select	ENSP00000311095.4:p.Trp425=
ENST00000310638.8:c.1275G=	ENSP00000311095.4:p.Trp425=
ENST00000371904.8:c.1278G=	ENSP00000360971.4:p.Trp426=
ENST00000371905.1:c.1275G=	ENSP00000360972.1:p.Trp425=
ENST00000462347.5:c.981G=	ENSP00000477495.1:p.Trp327=
ENST00000465874.5:c.*73G=	ENSP00000476368.1:n.*73G=
ENST00000468629.5:c.1127-158G=	ENSP00000476619.1:n.1127-158G=
ENST00000474458.5:c.743-158G=	ENSP00000476988.1:n.743-158G=
ENST00000475477.5:c.*82-158G=	ENSP00000476854.1:n.*82-158G=
NM_000778.3:c.1275G=	NP_000769.2:p.Trp425=
XM_005270539.1:c.981G=	XP_005270596.1:p.Trp327=
XM_011540826.1:c.1293G=	XP_011539128.1:p.Trp431=
XM_011540827.1:c.999G=	XP_011539129.1:p.Trp333=
XM_011540828.1:c.981G=	XP_011539130.1:p.Trp327=
XR_246241.1:n.1179G=
XR_246242.1:n.1163G=
NM_001319155.1:c.1179G=	NP_001306084.1:p.Trp393=
NM_001363587.1:c.981G=	NP_001350516.1:p.Trp327=
NR_134988.1:n.980G=
NR_134989.1:n.1171G=
NR_134990.1:n.1178-158G=
NR_134991.1:n.1152G=
NR_134992.1:n.794-158G=
NR_134993.1:n.928-158G=
NR_134994.1:n.1187G=
XM_017000465.1:c.963G=	XP_016855954.1:p.Trp321=
XR_001737005.1:n.1266-158G=
NM_000778.4:c.1275G= MANE Select	NP_000769.2:p.Trp425=
NM_001319155.2:c.1179G=	NP_001306084.1:p.Trp393=
NM_001363587.2:c.981G=	NP_001350516.1:p.Trp327=
NR_134988.2:n.972G=
NR_134989.2:n.1163G=
NR_134990.2:n.1170-158G=
NR_134991.2:n.1144G=
NR_134992.2:n.786-158G=
NR_134993.2:n.920-158G=
NR_134994.2:n.1179G=