Canonical Allele Identifier: CA340223264

Gene: CYP4A11

Linked Data

• MyVariant Identifiers: chr1:g.47398656T>A (hg19) ; chr1:g.46932984T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932984T>A , CM000663.2:g.46932984T>A	GRCh38
NC_000001.10:g.47398656T>A , CM000663.1:g.47398656T>A	GRCh37
NC_000001.9:g.47171243T>A	NCBI36
NG_007932.1:g.13501A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1286A>T MANE Select	ENSP00000311095.4:p.Glu429Val
ENST00000310638.8:c.1286A>T	ENSP00000311095.4:p.Glu429Val
ENST00000371904.8:c.1289A>T	ENSP00000360971.4:p.Glu430Val
ENST00000371905.1:c.1286A>T	ENSP00000360972.1:p.Glu429Val
ENST00000462347.5:c.992A>T	ENSP00000477495.1:p.Glu331Val
ENST00000465874.5:c.*84A>T	ENSP00000476368.1:n.*84A>T
ENST00000468629.5:c.1127-147A>T	ENSP00000476619.1:n.1127-147A>T
ENST00000474458.5:c.743-147A>T	ENSP00000476988.1:n.743-147A>T
ENST00000475477.5:c.*82-147A>T	ENSP00000476854.1:n.*82-147A>T
NM_000778.3:c.1286A>T	NP_000769.2:p.Glu429Val
XM_005270539.1:c.992A>T	XP_005270596.1:p.Glu331Val
XM_011540826.1:c.1304A>T	XP_011539128.1:p.Glu435Val
XM_011540827.1:c.1010A>T	XP_011539129.1:p.Glu337Val
XM_011540828.1:c.992A>T	XP_011539130.1:p.Glu331Val
XR_246241.1:n.1190A>T
XR_246242.1:n.1174A>T
NM_001319155.1:c.1190A>T	NP_001306084.1:p.Glu397Val
NM_001363587.1:c.992A>T	NP_001350516.1:p.Glu331Val
NR_134988.1:n.991A>T
NR_134989.1:n.1182A>T
NR_134990.1:n.1178-147A>T
NR_134991.1:n.1163A>T
NR_134992.1:n.794-147A>T
NR_134993.1:n.928-147A>T
NR_134994.1:n.1198A>T
XM_017000465.1:c.974A>T	XP_016855954.1:p.Glu325Val
XR_001737005.1:n.1266-147A>T
NM_000778.4:c.1286A>T MANE Select	NP_000769.2:p.Glu429Val
NM_001319155.2:c.1190A>T	NP_001306084.1:p.Glu397Val
NM_001363587.2:c.992A>T	NP_001350516.1:p.Glu331Val
NR_134988.2:n.983A>T
NR_134989.2:n.1174A>T
NR_134990.2:n.1170-147A>T
NR_134991.2:n.1155A>T
NR_134992.2:n.786-147A>T
NR_134993.2:n.920-147A>T
NR_134994.2:n.1190A>T