Canonical Allele Identifier: CA1140164580

Gene: CYP4A11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46931107A= , CM000663.2:g.46931107A=	GRCh38
NC_000001.10:g.47396779A= , CM000663.1:g.47396779A=	GRCh37
NC_000001.9:g.47169366A=	NCBI36
NG_007932.1:g.15378T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1365-797T= MANE Select	ENSP00000311095.4:n.1365-797T=
ENST00000310638.8:c.1365-797T=	ENSP00000311095.4:n.1365-797T=
ENST00000371904.8:c.1368-797T=	ENSP00000360971.4:n.1368-797T=
ENST00000462347.5:c.1071-797T=	ENSP00000477495.1:n.1071-797T=
ENST00000468629.5:c.*70-797T=	ENSP00000476619.1:n.*70-797T=
ENST00000474458.5:c.*70-797T=	ENSP00000476988.1:n.*70-797T=
ENST00000475477.5:c.*159-797T=	ENSP00000476854.1:n.*159-797T=
NM_000778.3:c.1365-797T=	NP_000769.2:n.1365-797T=
XM_011540826.1:c.1383-797T=	XP_011539128.1:n.1383-797T=
XM_011540827.1:c.1089-797T=	XP_011539129.1:n.1089-797T=
XM_011540828.1:c.1071-797T=	XP_011539130.1:n.1071-797T=
XR_246241.1:n.1269-797T=
XR_246242.1:n.1253-797T=
NM_001319155.1:c.1269-797T=	NP_001306084.1:n.1269-797T=
NM_001363587.1:c.1071-797T=	NP_001350516.1:n.1071-797T=
NR_134988.1:n.1070-797T=
NR_134989.1:n.1261-797T=
NR_134990.1:n.1255-797T=
NR_134991.1:n.1242-797T=
NR_134992.1:n.871-797T=
NR_134993.1:n.1005-797T=
NR_134994.1:n.1277-797T=
XM_017000465.1:c.1053-797T=	XP_016855954.1:n.1053-797T=
XR_001737005.1:n.1343-797T=
NM_000778.4:c.1365-797T= MANE Select	NP_000769.2:n.1365-797T=
NM_001319155.2:c.1269-797T=	NP_001306084.1:n.1269-797T=
NM_001363587.2:c.1071-797T=	NP_001350516.1:n.1071-797T=
NR_134988.2:n.1062-797T=
NR_134989.2:n.1253-797T=
NR_134990.2:n.1247-797T=
NR_134991.2:n.1234-797T=
NR_134992.2:n.863-797T=
NR_134993.2:n.997-797T=
NR_134994.2:n.1269-797T=