Canonical Allele Identifier: CA340223096

Gene: CYP4A11

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932762T>A , CM000663.2:g.46932762T>A	GRCh38
NC_000001.10:g.47398434T>A , CM000663.1:g.47398434T>A	GRCh37
NC_000001.9:g.47171021T>A	NCBI36
NG_007932.1:g.13723A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1363A>T MANE Select	ENSP00000311095.4:p.Arg455Trp
ENST00000310638.8:c.1363A>T	ENSP00000311095.4:p.Arg455Trp
ENST00000371904.8:c.1366A>T	ENSP00000360971.4:p.Arg456Trp
ENST00000371905.1:c.1363A>T	ENSP00000360972.1:p.Arg455Trp
ENST00000462347.5:c.1069A>T	ENSP00000477495.1:p.Arg357Trp
ENST00000465874.5:c.*161A>T	ENSP00000476368.1:n.*161A>T
ENST00000468629.5:c.*68A>T	ENSP00000476619.1:n.*68A>T
ENST00000474458.5:c.*68A>T	ENSP00000476988.1:n.*68A>T
ENST00000475477.5:c.*157A>T	ENSP00000476854.1:n.*157A>T
NM_000778.3:c.1363A>T	NP_000769.2:p.Arg455Trp
XM_005270539.1:c.1069A>T	XP_005270596.1:p.Arg357Trp
XM_011540826.1:c.1381A>T	XP_011539128.1:p.Arg461Trp
XM_011540827.1:c.1087A>T	XP_011539129.1:p.Arg363Trp
XM_011540828.1:c.1069A>T	XP_011539130.1:p.Arg357Trp
XR_246241.1:n.1267A>T
XR_246242.1:n.1251A>T
NM_001319155.1:c.1267A>T	NP_001306084.1:p.Arg423Trp
NM_001363587.1:c.1069A>T	NP_001350516.1:p.Arg357Trp
NR_134988.1:n.1068A>T
NR_134989.1:n.1259A>T
NR_134990.1:n.1253A>T
NR_134991.1:n.1240A>T
NR_134992.1:n.869A>T
NR_134993.1:n.1003A>T
NR_134994.1:n.1275A>T
XM_017000465.1:c.1051A>T	XP_016855954.1:p.Arg351Trp
XR_001737005.1:n.1341A>T
NM_000778.4:c.1363A>T MANE Select	NP_000769.2:p.Arg455Trp
NM_001319155.2:c.1267A>T	NP_001306084.1:p.Arg423Trp
NM_001363587.2:c.1069A>T	NP_001350516.1:p.Arg357Trp
NR_134988.2:n.1060A>T
NR_134989.2:n.1251A>T
NR_134990.2:n.1245A>T
NR_134991.2:n.1232A>T
NR_134992.2:n.861A>T
NR_134993.2:n.995A>T
NR_134994.2:n.1267A>T