Canonical Allele Identifier: CA340223293

Gene: CYP4A11

Linked Data

• dbSNP Id: rs2148454089
• MyVariant Identifiers: chr1:g.47398669A>T (hg19) ; chr1:g.46932997A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932997A>T , CM000663.2:g.46932997A>T	GRCh38
NC_000001.10:g.47398669A>T , CM000663.1:g.47398669A>T	GRCh37
NC_000001.9:g.47171256A>T	NCBI36
NG_007932.1:g.13488T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1273T>A MANE Select	ENSP00000311095.4:p.Trp425Arg
ENST00000310638.8:c.1273T>A	ENSP00000311095.4:p.Trp425Arg
ENST00000371904.8:c.1276T>A	ENSP00000360971.4:p.Trp426Arg
ENST00000371905.1:c.1273T>A	ENSP00000360972.1:p.Trp425Arg
ENST00000462347.5:c.979T>A	ENSP00000477495.1:p.Trp327Arg
ENST00000465874.5:c.*71T>A	ENSP00000476368.1:n.*71T>A
ENST00000468629.5:c.1127-160T>A	ENSP00000476619.1:n.1127-160T>A
ENST00000474458.5:c.743-160T>A	ENSP00000476988.1:n.743-160T>A
ENST00000475477.5:c.*82-160T>A	ENSP00000476854.1:n.*82-160T>A
NM_000778.3:c.1273T>A	NP_000769.2:p.Trp425Arg
XM_005270539.1:c.979T>A	XP_005270596.1:p.Trp327Arg
XM_011540826.1:c.1291T>A	XP_011539128.1:p.Trp431Arg
XM_011540827.1:c.997T>A	XP_011539129.1:p.Trp333Arg
XM_011540828.1:c.979T>A	XP_011539130.1:p.Trp327Arg
XR_246241.1:n.1177T>A
XR_246242.1:n.1161T>A
NM_001319155.1:c.1177T>A	NP_001306084.1:p.Trp393Arg
NM_001363587.1:c.979T>A	NP_001350516.1:p.Trp327Arg
NR_134988.1:n.978T>A
NR_134989.1:n.1169T>A
NR_134990.1:n.1178-160T>A
NR_134991.1:n.1150T>A
NR_134992.1:n.794-160T>A
NR_134993.1:n.928-160T>A
NR_134994.1:n.1185T>A
XM_017000465.1:c.961T>A	XP_016855954.1:p.Trp321Arg
XR_001737005.1:n.1266-160T>A
NM_000778.4:c.1273T>A MANE Select	NP_000769.2:p.Trp425Arg
NM_001319155.2:c.1177T>A	NP_001306084.1:p.Trp393Arg
NM_001363587.2:c.979T>A	NP_001350516.1:p.Trp327Arg
NR_134988.2:n.970T>A
NR_134989.2:n.1161T>A
NR_134990.2:n.1170-160T>A
NR_134991.2:n.1142T>A
NR_134992.2:n.786-160T>A
NR_134993.2:n.920-160T>A
NR_134994.2:n.1177T>A