Canonical Allele Identifier: CA417755909

Gene: CYP4A11

Linked Data

• dbSNP Id: rs1681109205
• MyVariant Identifiers: chr1:g.47398501G>A (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000310638.9:c.1296C>T MANE Select	ENSP00000311095.4:p.Asp432=
ENST00000310638.8:c.1296C>T	ENSP00000311095.4:p.Asp432=
ENST00000371904.8:c.1299C>T	ENSP00000360971.4:p.Asp433=
ENST00000371905.1:c.1296C>T	ENSP00000360972.1:p.Asp432=
ENST00000462347.5:c.1002C>T	ENSP00000477495.1:p.Asp334=
ENST00000465874.5:c.*94C>T	ENSP00000476368.1:n.*94C>T
ENST00000468629.5:c.*1C>T	ENSP00000476619.1:n.*1C>T
ENST00000474458.5:c.*1C>T	ENSP00000476988.1:n.*1C>T
ENST00000475477.5:c.*90C>T	ENSP00000476854.1:n.*90C>T
NM_000778.3:c.1296C>T	NP_000769.2:p.Asp432=
XM_005270539.1:c.1002C>T	XP_005270596.1:p.Asp334=
XM_011540826.1:c.1314C>T	XP_011539128.1:p.Asp438=
XM_011540827.1:c.1020C>T	XP_011539129.1:p.Asp340=
XM_011540828.1:c.1002C>T	XP_011539130.1:p.Asp334=
XR_246241.1:n.1200C>T
XR_246242.1:n.1184C>T
NM_001319155.1:c.1200C>T	NP_001306084.1:p.Asp400=
NM_001363587.1:c.1002C>T	NP_001350516.1:p.Asp334=
NR_134988.1:n.1001C>T
NR_134989.1:n.1192C>T
NR_134990.1:n.1186C>T
NR_134991.1:n.1173C>T
NR_134992.1:n.802C>T
NR_134993.1:n.936C>T
NR_134994.1:n.1208C>T
XM_017000465.1:c.984C>T	XP_016855954.1:p.Asp328=
XR_001737005.1:n.1274C>T
NM_000778.4:c.1296C>T MANE Select	NP_000769.2:p.Asp432=
NM_001319155.2:c.1200C>T	NP_001306084.1:p.Asp400=
NM_001363587.2:c.1002C>T	NP_001350516.1:p.Asp334=
NR_134988.2:n.993C>T
NR_134989.2:n.1184C>T
NR_134990.2:n.1178C>T
NR_134991.2:n.1165C>T
NR_134992.2:n.794C>T
NR_134993.2:n.928C>T
NR_134994.2:n.1200C>T