Canonical Allele Identifier: CA417755727

Gene: CYP4A11

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932763T>G , CM000663.2:g.46932763T>G	GRCh38
NC_000001.10:g.47398435T>G , CM000663.1:g.47398435T>G	GRCh37
NC_000001.9:g.47171022T>G	NCBI36
NG_007932.1:g.13722A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1362A>C MANE Select	ENSP00000311095.4:p.Ser454=
ENST00000310638.8:c.1362A>C	ENSP00000311095.4:p.Ser454=
ENST00000371904.8:c.1365A>C	ENSP00000360971.4:p.Ser455=
ENST00000371905.1:c.1362A>C	ENSP00000360972.1:p.Ser454=
ENST00000462347.5:c.1068A>C	ENSP00000477495.1:p.Ser356=
ENST00000465874.5:c.*160A>C	ENSP00000476368.1:n.*160A>C
ENST00000468629.5:c.*67A>C	ENSP00000476619.1:n.*67A>C
ENST00000474458.5:c.*67A>C	ENSP00000476988.1:n.*67A>C
ENST00000475477.5:c.*156A>C	ENSP00000476854.1:n.*156A>C
NM_000778.3:c.1362A>C	NP_000769.2:p.Ser454=
XM_005270539.1:c.1068A>C	XP_005270596.1:p.Ser356=
XM_011540826.1:c.1380A>C	XP_011539128.1:p.Ser460=
XM_011540827.1:c.1086A>C	XP_011539129.1:p.Ser362=
XM_011540828.1:c.1068A>C	XP_011539130.1:p.Ser356=
XR_246241.1:n.1266A>C
XR_246242.1:n.1250A>C
NM_001319155.1:c.1266A>C	NP_001306084.1:p.Ser422=
NM_001363587.1:c.1068A>C	NP_001350516.1:p.Ser356=
NR_134988.1:n.1067A>C
NR_134989.1:n.1258A>C
NR_134990.1:n.1252A>C
NR_134991.1:n.1239A>C
NR_134992.1:n.868A>C
NR_134993.1:n.1002A>C
NR_134994.1:n.1274A>C
XM_017000465.1:c.1050A>C	XP_016855954.1:p.Ser350=
XR_001737005.1:n.1340A>C
NM_000778.4:c.1362A>C MANE Select	NP_000769.2:p.Ser454=
NM_001319155.2:c.1266A>C	NP_001306084.1:p.Ser422=
NM_001363587.2:c.1068A>C	NP_001350516.1:p.Ser356=
NR_134988.2:n.1059A>C
NR_134989.2:n.1250A>C
NR_134990.2:n.1244A>C
NR_134991.2:n.1231A>C
NR_134992.2:n.860A>C
NR_134993.2:n.994A>C
NR_134994.2:n.1266A>C