Canonical Allele Identifier: CA2474390684

Gene: CYP4A11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932965C= , CM000663.2:g.46932965C=	GRCh38
NC_000001.10:g.47398637C= , CM000663.1:g.47398637C=	GRCh37
NC_000001.9:g.47171224C=	NCBI36
NG_007932.1:g.13520G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1287+18G= MANE Select	ENSP00000311095.4:n.1287+18G=
ENST00000310638.8:c.1287+18G=	ENSP00000311095.4:n.1287+18G=
ENST00000371904.8:c.1290+18G=	ENSP00000360971.4:n.1290+18G=
ENST00000371905.1:c.1287+18G=	ENSP00000360972.1:n.1287+18G=
ENST00000462347.5:c.993+18G=	ENSP00000477495.1:n.993+18G=
ENST00000465874.5:c.*85+18G=	ENSP00000476368.1:n.*85+18G=
ENST00000468629.5:c.1127-128G=	ENSP00000476619.1:n.1127-128G=
ENST00000474458.5:c.743-128G=	ENSP00000476988.1:n.743-128G=
ENST00000475477.5:c.*82-128G=	ENSP00000476854.1:n.*82-128G=
NM_000778.3:c.1287+18G=	NP_000769.2:n.1287+18G=
XM_005270539.1:c.993+18G=	XP_005270596.1:n.993+18G=
XM_011540826.1:c.1305+18G=	XP_011539128.1:n.1305+18G=
XM_011540827.1:c.1011+18G=	XP_011539129.1:n.1011+18G=
XM_011540828.1:c.993+18G=	XP_011539130.1:n.993+18G=
XR_246241.1:n.1191+18G=
XR_246242.1:n.1175+18G=
NM_001319155.1:c.1191+18G=	NP_001306084.1:n.1191+18G=
NM_001363587.1:c.993+18G=	NP_001350516.1:n.993+18G=
NR_134988.1:n.992+18G=
NR_134989.1:n.1183+18G=
NR_134990.1:n.1178-128G=
NR_134991.1:n.1164+18G=
NR_134992.1:n.794-128G=
NR_134993.1:n.928-128G=
NR_134994.1:n.1199+18G=
XM_017000465.1:c.975+18G=	XP_016855954.1:n.975+18G=
XR_001737005.1:n.1266-128G=
NM_000778.4:c.1287+18G= MANE Select	NP_000769.2:n.1287+18G=
NM_001319155.2:c.1191+18G=	NP_001306084.1:n.1191+18G=
NM_001363587.2:c.993+18G=	NP_001350516.1:n.993+18G=
NR_134988.2:n.984+18G=
NR_134989.2:n.1175+18G=
NR_134990.2:n.1170-128G=
NR_134991.2:n.1156+18G=
NR_134992.2:n.786-128G=
NR_134993.2:n.920-128G=
NR_134994.2:n.1191+18G=