Canonical Allele Identifier: CA2474389842

Gene: CYP4A11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46930998C= , CM000663.2:g.46930998C=	GRCh38
NC_000001.10:g.47396670C= , CM000663.1:g.47396670C=	GRCh37
NC_000001.9:g.47169257C=	NCBI36
NG_007932.1:g.15487G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1365-688G= MANE Select	ENSP00000311095.4:n.1365-688G=
ENST00000310638.8:c.1365-688G=	ENSP00000311095.4:n.1365-688G=
ENST00000371904.8:c.1368-688G=	ENSP00000360971.4:n.1368-688G=
ENST00000462347.5:c.1071-688G=	ENSP00000477495.1:n.1071-688G=
ENST00000468629.5:c.*70-688G=	ENSP00000476619.1:n.*70-688G=
ENST00000474458.5:c.*70-688G=	ENSP00000476988.1:n.*70-688G=
ENST00000475477.5:c.*159-688G=	ENSP00000476854.1:n.*159-688G=
NM_000778.3:c.1365-688G=	NP_000769.2:n.1365-688G=
XM_011540826.1:c.1383-688G=	XP_011539128.1:n.1383-688G=
XM_011540827.1:c.1089-688G=	XP_011539129.1:n.1089-688G=
XM_011540828.1:c.1071-688G=	XP_011539130.1:n.1071-688G=
XR_246241.1:n.1269-688G=
XR_246242.1:n.1253-688G=
NM_001319155.1:c.1269-688G=	NP_001306084.1:n.1269-688G=
NM_001363587.1:c.1071-688G=	NP_001350516.1:n.1071-688G=
NR_134988.1:n.1070-688G=
NR_134989.1:n.1261-688G=
NR_134990.1:n.1255-688G=
NR_134991.1:n.1242-688G=
NR_134992.1:n.871-688G=
NR_134993.1:n.1005-688G=
NR_134994.1:n.1277-688G=
XM_017000465.1:c.1053-688G=	XP_016855954.1:n.1053-688G=
XR_001737005.1:n.1343-688G=
NM_000778.4:c.1365-688G= MANE Select	NP_000769.2:n.1365-688G=
NM_001319155.2:c.1269-688G=	NP_001306084.1:n.1269-688G=
NM_001363587.2:c.1071-688G=	NP_001350516.1:n.1071-688G=
NR_134988.2:n.1062-688G=
NR_134989.2:n.1253-688G=
NR_134990.2:n.1247-688G=
NR_134991.2:n.1234-688G=
NR_134992.2:n.863-688G=
NR_134993.2:n.997-688G=
NR_134994.2:n.1269-688G=