Canonical Allele Identifier: CA340223249

Gene: CYP4A11

Linked Data

• MyVariant Identifiers: chr1:g.47398508A>T (hg19) ; chr1:g.46932836A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932836A>T , CM000663.2:g.46932836A>T	GRCh38
NC_000001.10:g.47398508A>T , CM000663.1:g.47398508A>T	GRCh37
NC_000001.9:g.47171095A>T	NCBI36
NG_007932.1:g.13649T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000310638.9:c.1289T>A MANE Select	ENSP00000311095.4:p.Val430Glu
ENST00000310638.8:c.1289T>A	ENSP00000311095.4:p.Val430Glu
ENST00000371904.8:c.1292T>A	ENSP00000360971.4:p.Val431Glu
ENST00000371905.1:c.1289T>A	ENSP00000360972.1:p.Val430Glu
ENST00000462347.5:c.995T>A	ENSP00000477495.1:p.Val332Glu
ENST00000465874.5:c.*87T>A	ENSP00000476368.1:n.*87T>A
ENST00000468629.5:c.1128T>A	ENSP00000476619.1:p.Gly376=
ENST00000474458.5:c.744T>A	ENSP00000476988.1:p.Ser248Arg
ENST00000475477.5:c.*83T>A	ENSP00000476854.1:n.*83T>A
NM_000778.3:c.1289T>A	NP_000769.2:p.Val430Glu
XM_005270539.1:c.995T>A	XP_005270596.1:p.Val332Glu
XM_011540826.1:c.1307T>A	XP_011539128.1:p.Val436Glu
XM_011540827.1:c.1013T>A	XP_011539129.1:p.Val338Glu
XM_011540828.1:c.995T>A	XP_011539130.1:p.Val332Glu
XR_246241.1:n.1193T>A
XR_246242.1:n.1177T>A
NM_001319155.1:c.1193T>A	NP_001306084.1:p.Val398Glu
NM_001363587.1:c.995T>A	NP_001350516.1:p.Val332Glu
NR_134988.1:n.994T>A
NR_134989.1:n.1185T>A
NR_134990.1:n.1179T>A
NR_134991.1:n.1166T>A
NR_134992.1:n.795T>A
NR_134993.1:n.929T>A
NR_134994.1:n.1201T>A
XM_017000465.1:c.977T>A	XP_016855954.1:p.Val326Glu
XR_001737005.1:n.1267T>A
NM_000778.4:c.1289T>A MANE Select	NP_000769.2:p.Val430Glu
NM_001319155.2:c.1193T>A	NP_001306084.1:p.Val398Glu
NM_001363587.2:c.995T>A	NP_001350516.1:p.Val332Glu
NR_134988.2:n.986T>A
NR_134989.2:n.1177T>A
NR_134990.2:n.1171T>A
NR_134991.2:n.1158T>A
NR_134992.2:n.787T>A
NR_134993.2:n.921T>A
NR_134994.2:n.1193T>A