Canonical Allele Identifier: CA340223233

Gene: CYP4A11

Linked Data

• MyVariant Identifiers: chr1:g.47398501G>T (hg19) ; chr1:g.46932829G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932829G>T , CM000663.2:g.46932829G>T	GRCh38
NC_000001.10:g.47398501G>T , CM000663.1:g.47398501G>T	GRCh37
NC_000001.9:g.47171088G>T	NCBI36
NG_007932.1:g.13656C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000310638.9:c.1296C>A MANE Select	ENSP00000311095.4:p.Asp432Glu
ENST00000310638.8:c.1296C>A	ENSP00000311095.4:p.Asp432Glu
ENST00000371904.8:c.1299C>A	ENSP00000360971.4:p.Asp433Glu
ENST00000371905.1:c.1296C>A	ENSP00000360972.1:p.Asp432Glu
ENST00000462347.5:c.1002C>A	ENSP00000477495.1:p.Asp334Glu
ENST00000465874.5:c.*94C>A	ENSP00000476368.1:n.*94C>A
ENST00000468629.5:c.*1C>A	ENSP00000476619.1:n.*1C>A
ENST00000474458.5:c.*1C>A	ENSP00000476988.1:n.*1C>A
ENST00000475477.5:c.*90C>A	ENSP00000476854.1:n.*90C>A
NM_000778.3:c.1296C>A	NP_000769.2:p.Asp432Glu
XM_005270539.1:c.1002C>A	XP_005270596.1:p.Asp334Glu
XM_011540826.1:c.1314C>A	XP_011539128.1:p.Asp438Glu
XM_011540827.1:c.1020C>A	XP_011539129.1:p.Asp340Glu
XM_011540828.1:c.1002C>A	XP_011539130.1:p.Asp334Glu
XR_246241.1:n.1200C>A
XR_246242.1:n.1184C>A
NM_001319155.1:c.1200C>A	NP_001306084.1:p.Asp400Glu
NM_001363587.1:c.1002C>A	NP_001350516.1:p.Asp334Glu
NR_134988.1:n.1001C>A
NR_134989.1:n.1192C>A
NR_134990.1:n.1186C>A
NR_134991.1:n.1173C>A
NR_134992.1:n.802C>A
NR_134993.1:n.936C>A
NR_134994.1:n.1208C>A
XM_017000465.1:c.984C>A	XP_016855954.1:p.Asp328Glu
XR_001737005.1:n.1274C>A
NM_000778.4:c.1296C>A MANE Select	NP_000769.2:p.Asp432Glu
NM_001319155.2:c.1200C>A	NP_001306084.1:p.Asp400Glu
NM_001363587.2:c.1002C>A	NP_001350516.1:p.Asp334Glu
NR_134988.2:n.993C>A
NR_134989.2:n.1184C>A
NR_134990.2:n.1178C>A
NR_134991.2:n.1165C>A
NR_134992.2:n.794C>A
NR_134993.2:n.928C>A
NR_134994.2:n.1200C>A