Canonical Allele Identifier: CA1143797786

Gene: CYP4A11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46933216G= , CM000663.2:g.46933216G=	GRCh38
NC_000001.10:g.47398888G= , CM000663.1:g.47398888G=	GRCh37
NC_000001.9:g.47171475G=	NCBI36
NG_007932.1:g.13269C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1223-169C= MANE Select	ENSP00000311095.4:n.1223-169C=
ENST00000310638.8:c.1223-169C=	ENSP00000311095.4:n.1223-169C=
ENST00000371904.8:c.1226-169C=	ENSP00000360971.4:n.1226-169C=
ENST00000371905.1:c.1223-169C=	ENSP00000360972.1:n.1223-169C=
ENST00000462347.5:c.929-169C=	ENSP00000477495.1:n.929-169C=
ENST00000465874.5:c.*21-169C=	ENSP00000476368.1:n.*21-169C=
ENST00000468629.5:c.1127-379C=	ENSP00000476619.1:n.1127-379C=
ENST00000474458.5:c.743-379C=	ENSP00000476988.1:n.743-379C=
ENST00000475477.5:c.*82-379C=	ENSP00000476854.1:n.*82-379C=
NM_000778.3:c.1223-169C=	NP_000769.2:n.1223-169C=
XM_005270539.1:c.929-169C=	XP_005270596.1:n.929-169C=
XM_011540826.1:c.1241-169C=	XP_011539128.1:n.1241-169C=
XM_011540827.1:c.947-169C=	XP_011539129.1:n.947-169C=
XM_011540828.1:c.929-169C=	XP_011539130.1:n.929-169C=
XR_246241.1:n.1127-169C=
XR_246242.1:n.1111-169C=
NM_001319155.1:c.1127-169C=	NP_001306084.1:n.1127-169C=
NM_001363587.1:c.929-169C=	NP_001350516.1:n.929-169C=
NR_134988.1:n.928-169C=
NR_134989.1:n.1119-169C=
NR_134990.1:n.1178-379C=
NR_134991.1:n.1100-169C=
NR_134992.1:n.794-379C=
NR_134993.1:n.928-379C=
NR_134994.1:n.1135-169C=
XM_017000465.1:c.911-169C=	XP_016855954.1:n.911-169C=
XR_001737005.1:n.1266-379C=
NM_000778.4:c.1223-169C= MANE Select	NP_000769.2:n.1223-169C=
NM_001319155.2:c.1127-169C=	NP_001306084.1:n.1127-169C=
NM_001363587.2:c.929-169C=	NP_001350516.1:n.929-169C=
NR_134988.2:n.920-169C=
NR_134989.2:n.1111-169C=
NR_134990.2:n.1170-379C=
NR_134991.2:n.1092-169C=
NR_134992.2:n.786-379C=
NR_134993.2:n.920-379C=
NR_134994.2:n.1127-169C=