Canonical Allele Identifier: CA2474390808

Gene: CYP4A11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46933238C= , CM000663.2:g.46933238C=	GRCh38
NC_000001.10:g.47398910C= , CM000663.1:g.47398910C=	GRCh37
NC_000001.9:g.47171497C=	NCBI36
NG_007932.1:g.13247G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1223-191G= MANE Select	ENSP00000311095.4:n.1223-191G=
ENST00000310638.8:c.1223-191G=	ENSP00000311095.4:n.1223-191G=
ENST00000371904.8:c.1226-191G=	ENSP00000360971.4:n.1226-191G=
ENST00000371905.1:c.1223-191G=	ENSP00000360972.1:n.1223-191G=
ENST00000462347.5:c.929-191G=	ENSP00000477495.1:n.929-191G=
ENST00000465874.5:c.*21-191G=	ENSP00000476368.1:n.*21-191G=
ENST00000468629.5:c.1127-401G=	ENSP00000476619.1:n.1127-401G=
ENST00000474458.5:c.743-401G=	ENSP00000476988.1:n.743-401G=
ENST00000475477.5:c.*82-401G=	ENSP00000476854.1:n.*82-401G=
NM_000778.3:c.1223-191G=	NP_000769.2:n.1223-191G=
XM_005270539.1:c.929-191G=	XP_005270596.1:n.929-191G=
XM_011540826.1:c.1241-191G=	XP_011539128.1:n.1241-191G=
XM_011540827.1:c.947-191G=	XP_011539129.1:n.947-191G=
XM_011540828.1:c.929-191G=	XP_011539130.1:n.929-191G=
XR_246241.1:n.1127-191G=
XR_246242.1:n.1111-191G=
NM_001319155.1:c.1127-191G=	NP_001306084.1:n.1127-191G=
NM_001363587.1:c.929-191G=	NP_001350516.1:n.929-191G=
NR_134988.1:n.928-191G=
NR_134989.1:n.1119-191G=
NR_134990.1:n.1178-401G=
NR_134991.1:n.1100-191G=
NR_134992.1:n.794-401G=
NR_134993.1:n.928-401G=
NR_134994.1:n.1135-191G=
XM_017000465.1:c.911-191G=	XP_016855954.1:n.911-191G=
XR_001737005.1:n.1266-401G=
NM_000778.4:c.1223-191G= MANE Select	NP_000769.2:n.1223-191G=
NM_001319155.2:c.1127-191G=	NP_001306084.1:n.1127-191G=
NM_001363587.2:c.929-191G=	NP_001350516.1:n.929-191G=
NR_134988.2:n.920-191G=
NR_134989.2:n.1111-191G=
NR_134990.2:n.1170-401G=
NR_134991.2:n.1092-191G=
NR_134992.2:n.786-401G=
NR_134993.2:n.920-401G=
NR_134994.2:n.1127-191G=