Canonical Allele Identifier: CA2474389983

Gene: CYP4A11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46931289A= , CM000663.2:g.46931289A=	GRCh38
NC_000001.10:g.47396961A= , CM000663.1:g.47396961A=	GRCh37
NC_000001.9:g.47169548A=	NCBI36
NG_007932.1:g.15196T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1365-979T= MANE Select	ENSP00000311095.4:n.1365-979T=
ENST00000310638.8:c.1365-979T=	ENSP00000311095.4:n.1365-979T=
ENST00000371904.8:c.1368-979T=	ENSP00000360971.4:n.1368-979T=
ENST00000462347.5:c.1071-979T=	ENSP00000477495.1:n.1071-979T=
ENST00000468629.5:c.*70-979T=	ENSP00000476619.1:n.*70-979T=
ENST00000474458.5:c.*70-979T=	ENSP00000476988.1:n.*70-979T=
ENST00000475477.5:c.*159-979T=	ENSP00000476854.1:n.*159-979T=
NM_000778.3:c.1365-979T=	NP_000769.2:n.1365-979T=
XM_011540826.1:c.1383-979T=	XP_011539128.1:n.1383-979T=
XM_011540827.1:c.1089-979T=	XP_011539129.1:n.1089-979T=
XM_011540828.1:c.1071-979T=	XP_011539130.1:n.1071-979T=
XR_246241.1:n.1269-979T=
XR_246242.1:n.1253-979T=
NM_001319155.1:c.1269-979T=	NP_001306084.1:n.1269-979T=
NM_001363587.1:c.1071-979T=	NP_001350516.1:n.1071-979T=
NR_134988.1:n.1070-979T=
NR_134989.1:n.1261-979T=
NR_134990.1:n.1255-979T=
NR_134991.1:n.1242-979T=
NR_134992.1:n.871-979T=
NR_134993.1:n.1005-979T=
NR_134994.1:n.1277-979T=
XM_017000465.1:c.1053-979T=	XP_016855954.1:n.1053-979T=
XR_001737005.1:n.1343-979T=
NM_000778.4:c.1365-979T= MANE Select	NP_000769.2:n.1365-979T=
NM_001319155.2:c.1269-979T=	NP_001306084.1:n.1269-979T=
NM_001363587.2:c.1071-979T=	NP_001350516.1:n.1071-979T=
NR_134988.2:n.1062-979T=
NR_134989.2:n.1253-979T=
NR_134990.2:n.1247-979T=
NR_134991.2:n.1234-979T=
NR_134992.2:n.863-979T=
NR_134993.2:n.997-979T=
NR_134994.2:n.1269-979T=