Canonical Allele Identifier: CA340223127

Gene: CYP4A11

Linked Data

• MyVariant Identifiers: chr1:g.47398449A>T (hg19) ; chr1:g.46932777A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932777A>T , CM000663.2:g.46932777A>T	GRCh38
NC_000001.10:g.47398449A>T , CM000663.1:g.47398449A>T	GRCh37
NC_000001.9:g.47171036A>T	NCBI36
NG_007932.1:g.13708T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000310638.9:c.1348T>A MANE Select	ENSP00000311095.4:p.Phe450Ile
ENST00000310638.8:c.1348T>A	ENSP00000311095.4:p.Phe450Ile
ENST00000371904.8:c.1351T>A	ENSP00000360971.4:p.Phe451Ile
ENST00000371905.1:c.1348T>A	ENSP00000360972.1:p.Phe450Ile
ENST00000462347.5:c.1054T>A	ENSP00000477495.1:p.Phe352Ile
ENST00000465874.5:c.*146T>A	ENSP00000476368.1:n.*146T>A
ENST00000468629.5:c.*53T>A	ENSP00000476619.1:n.*53T>A
ENST00000474458.5:c.*53T>A	ENSP00000476988.1:n.*53T>A
ENST00000475477.5:c.*142T>A	ENSP00000476854.1:n.*142T>A
NM_000778.3:c.1348T>A	NP_000769.2:p.Phe450Ile
XM_005270539.1:c.1054T>A	XP_005270596.1:p.Phe352Ile
XM_011540826.1:c.1366T>A	XP_011539128.1:p.Phe456Ile
XM_011540827.1:c.1072T>A	XP_011539129.1:p.Phe358Ile
XM_011540828.1:c.1054T>A	XP_011539130.1:p.Phe352Ile
XR_246241.1:n.1252T>A
XR_246242.1:n.1236T>A
NM_001319155.1:c.1252T>A	NP_001306084.1:p.Phe418Ile
NM_001363587.1:c.1054T>A	NP_001350516.1:p.Phe352Ile
NR_134988.1:n.1053T>A
NR_134989.1:n.1244T>A
NR_134990.1:n.1238T>A
NR_134991.1:n.1225T>A
NR_134992.1:n.854T>A
NR_134993.1:n.988T>A
NR_134994.1:n.1260T>A
XM_017000465.1:c.1036T>A	XP_016855954.1:p.Phe346Ile
XR_001737005.1:n.1326T>A
NM_000778.4:c.1348T>A MANE Select	NP_000769.2:p.Phe450Ile
NM_001319155.2:c.1252T>A	NP_001306084.1:p.Phe418Ile
NM_001363587.2:c.1054T>A	NP_001350516.1:p.Phe352Ile
NR_134988.2:n.1045T>A
NR_134989.2:n.1236T>A
NR_134990.2:n.1230T>A
NR_134991.2:n.1217T>A
NR_134992.2:n.846T>A
NR_134993.2:n.980T>A
NR_134994.2:n.1252T>A