Canonical Allele Identifier: CA340223182

Gene: CYP4A11

Linked Data

• MyVariant Identifiers: chr1:g.47398475G>A (hg19) ; chr1:g.46932803G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932803G>A , CM000663.2:g.46932803G>A	GRCh38
NC_000001.10:g.47398475G>A , CM000663.1:g.47398475G>A	GRCh37
NC_000001.9:g.47171062G>A	NCBI36
NG_007932.1:g.13682C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1322C>T MANE Select	ENSP00000311095.4:p.Ala441Val
ENST00000310638.8:c.1322C>T	ENSP00000311095.4:p.Ala441Val
ENST00000371904.8:c.1325C>T	ENSP00000360971.4:p.Ala442Val
ENST00000371905.1:c.1322C>T	ENSP00000360972.1:p.Ala441Val
ENST00000462347.5:c.1028C>T	ENSP00000477495.1:p.Ala343Val
ENST00000465874.5:c.*120C>T	ENSP00000476368.1:n.*120C>T
ENST00000468629.5:c.*27C>T	ENSP00000476619.1:n.*27C>T
ENST00000474458.5:c.*27C>T	ENSP00000476988.1:n.*27C>T
ENST00000475477.5:c.*116C>T	ENSP00000476854.1:n.*116C>T
NM_000778.3:c.1322C>T	NP_000769.2:p.Ala441Val
XM_005270539.1:c.1028C>T	XP_005270596.1:p.Ala343Val
XM_011540826.1:c.1340C>T	XP_011539128.1:p.Ala447Val
XM_011540827.1:c.1046C>T	XP_011539129.1:p.Ala349Val
XM_011540828.1:c.1028C>T	XP_011539130.1:p.Ala343Val
XR_246241.1:n.1226C>T
XR_246242.1:n.1210C>T
NM_001319155.1:c.1226C>T	NP_001306084.1:p.Ala409Val
NM_001363587.1:c.1028C>T	NP_001350516.1:p.Ala343Val
NR_134988.1:n.1027C>T
NR_134989.1:n.1218C>T
NR_134990.1:n.1212C>T
NR_134991.1:n.1199C>T
NR_134992.1:n.828C>T
NR_134993.1:n.962C>T
NR_134994.1:n.1234C>T
XM_017000465.1:c.1010C>T	XP_016855954.1:p.Ala337Val
XR_001737005.1:n.1300C>T
NM_000778.4:c.1322C>T MANE Select	NP_000769.2:p.Ala441Val
NM_001319155.2:c.1226C>T	NP_001306084.1:p.Ala409Val
NM_001363587.2:c.1028C>T	NP_001350516.1:p.Ala343Val
NR_134988.2:n.1019C>T
NR_134989.2:n.1210C>T
NR_134990.2:n.1204C>T
NR_134991.2:n.1191C>T
NR_134992.2:n.820C>T
NR_134993.2:n.954C>T
NR_134994.2:n.1226C>T