Canonical Allele Identifier: CA340223213

Gene: CYP4A11

Linked Data

• MyVariant Identifiers: chr1:g.47398490A>T (hg19) ; chr1:g.46932818A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932818A>T , CM000663.2:g.46932818A>T	GRCh38
NC_000001.10:g.47398490A>T , CM000663.1:g.47398490A>T	GRCh37
NC_000001.9:g.47171077A>T	NCBI36
NG_007932.1:g.13667T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1307T>A MANE Select	ENSP00000311095.4:p.Phe436Tyr
ENST00000310638.8:c.1307T>A	ENSP00000311095.4:p.Phe436Tyr
ENST00000371904.8:c.1310T>A	ENSP00000360971.4:p.Phe437Tyr
ENST00000371905.1:c.1307T>A	ENSP00000360972.1:p.Phe436Tyr
ENST00000462347.5:c.1013T>A	ENSP00000477495.1:p.Phe338Tyr
ENST00000465874.5:c.*105T>A	ENSP00000476368.1:n.*105T>A
ENST00000468629.5:c.*12T>A	ENSP00000476619.1:n.*12T>A
ENST00000474458.5:c.*12T>A	ENSP00000476988.1:n.*12T>A
ENST00000475477.5:c.*101T>A	ENSP00000476854.1:n.*101T>A
NM_000778.3:c.1307T>A	NP_000769.2:p.Phe436Tyr
XM_005270539.1:c.1013T>A	XP_005270596.1:p.Phe338Tyr
XM_011540826.1:c.1325T>A	XP_011539128.1:p.Phe442Tyr
XM_011540827.1:c.1031T>A	XP_011539129.1:p.Phe344Tyr
XM_011540828.1:c.1013T>A	XP_011539130.1:p.Phe338Tyr
XR_246241.1:n.1211T>A
XR_246242.1:n.1195T>A
NM_001319155.1:c.1211T>A	NP_001306084.1:p.Phe404Tyr
NM_001363587.1:c.1013T>A	NP_001350516.1:p.Phe338Tyr
NR_134988.1:n.1012T>A
NR_134989.1:n.1203T>A
NR_134990.1:n.1197T>A
NR_134991.1:n.1184T>A
NR_134992.1:n.813T>A
NR_134993.1:n.947T>A
NR_134994.1:n.1219T>A
XM_017000465.1:c.995T>A	XP_016855954.1:p.Phe332Tyr
XR_001737005.1:n.1285T>A
NM_000778.4:c.1307T>A MANE Select	NP_000769.2:p.Phe436Tyr
NM_001319155.2:c.1211T>A	NP_001306084.1:p.Phe404Tyr
NM_001363587.2:c.1013T>A	NP_001350516.1:p.Phe338Tyr
NR_134988.2:n.1004T>A
NR_134989.2:n.1195T>A
NR_134990.2:n.1189T>A
NR_134991.2:n.1176T>A
NR_134992.2:n.805T>A
NR_134993.2:n.939T>A
NR_134994.2:n.1211T>A