Canonical Allele Identifier: CA2474390632

Gene: CYP4A11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932875C= , CM000663.2:g.46932875C=	GRCh38
NC_000001.10:g.47398547C= , CM000663.1:g.47398547C=	GRCh37
NC_000001.9:g.47171134C=	NCBI36
NG_007932.1:g.13610G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000310638.9:c.1288-38G= MANE Select	ENSP00000311095.4:n.1288-38G=
ENST00000310638.8:c.1288-38G=	ENSP00000311095.4:n.1288-38G=
ENST00000371904.8:c.1291-38G=	ENSP00000360971.4:n.1291-38G=
ENST00000371905.1:c.1288-38G=	ENSP00000360972.1:n.1288-38G=
ENST00000462347.5:c.994-38G=	ENSP00000477495.1:n.994-38G=
ENST00000465874.5:c.*86-38G=	ENSP00000476368.1:n.*86-38G=
ENST00000468629.5:c.1127-38G=	ENSP00000476619.1:n.1127-38G=
ENST00000474458.5:c.743-38G=	ENSP00000476988.1:n.743-38G=
ENST00000475477.5:c.*82-38G=	ENSP00000476854.1:n.*82-38G=
NM_000778.3:c.1288-38G=	NP_000769.2:n.1288-38G=
XM_005270539.1:c.994-38G=	XP_005270596.1:n.994-38G=
XM_011540826.1:c.1306-38G=	XP_011539128.1:n.1306-38G=
XM_011540827.1:c.1012-38G=	XP_011539129.1:n.1012-38G=
XM_011540828.1:c.994-38G=	XP_011539130.1:n.994-38G=
XR_246241.1:n.1192-38G=
XR_246242.1:n.1176-38G=
NM_001319155.1:c.1192-38G=	NP_001306084.1:n.1192-38G=
NM_001363587.1:c.994-38G=	NP_001350516.1:n.994-38G=
NR_134988.1:n.993-38G=
NR_134989.1:n.1184-38G=
NR_134990.1:n.1178-38G=
NR_134991.1:n.1165-38G=
NR_134992.1:n.794-38G=
NR_134993.1:n.928-38G=
NR_134994.1:n.1200-38G=
XM_017000465.1:c.976-38G=	XP_016855954.1:n.976-38G=
XR_001737005.1:n.1266-38G=
NM_000778.4:c.1288-38G= MANE Select	NP_000769.2:n.1288-38G=
NM_001319155.2:c.1192-38G=	NP_001306084.1:n.1192-38G=
NM_001363587.2:c.994-38G=	NP_001350516.1:n.994-38G=
NR_134988.2:n.985-38G=
NR_134989.2:n.1176-38G=
NR_134990.2:n.1170-38G=
NR_134991.2:n.1157-38G=
NR_134992.2:n.786-38G=
NR_134993.2:n.920-38G=
NR_134994.2:n.1192-38G=