Canonical Allele Identifier: CA340223246

Gene: CYP4A11

Linked Data

• MyVariant Identifiers: chr1:g.47398506A>C (hg19) ; chr1:g.46932834A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932834A>C , CM000663.2:g.46932834A>C	GRCh38
NC_000001.10:g.47398506A>C , CM000663.1:g.47398506A>C	GRCh37
NC_000001.9:g.47171093A>C	NCBI36
NG_007932.1:g.13651T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000310638.9:c.1291T>G MANE Select	ENSP00000311095.4:p.Phe431Val
ENST00000310638.8:c.1291T>G	ENSP00000311095.4:p.Phe431Val
ENST00000371904.8:c.1294T>G	ENSP00000360971.4:p.Phe432Val
ENST00000371905.1:c.1291T>G	ENSP00000360972.1:p.Phe431Val
ENST00000462347.5:c.997T>G	ENSP00000477495.1:p.Phe333Val
ENST00000465874.5:c.*89T>G	ENSP00000476368.1:n.*89T>G
ENST00000468629.5:c.1130T>G	ENSP00000476619.1:p.Val377Gly
ENST00000474458.5:c.746T>G	ENSP00000476988.1:p.Val249Gly
ENST00000475477.5:c.*85T>G	ENSP00000476854.1:n.*85T>G
NM_000778.3:c.1291T>G	NP_000769.2:p.Phe431Val
XM_005270539.1:c.997T>G	XP_005270596.1:p.Phe333Val
XM_011540826.1:c.1309T>G	XP_011539128.1:p.Phe437Val
XM_011540827.1:c.1015T>G	XP_011539129.1:p.Phe339Val
XM_011540828.1:c.997T>G	XP_011539130.1:p.Phe333Val
XR_246241.1:n.1195T>G
XR_246242.1:n.1179T>G
NM_001319155.1:c.1195T>G	NP_001306084.1:p.Phe399Val
NM_001363587.1:c.997T>G	NP_001350516.1:p.Phe333Val
NR_134988.1:n.996T>G
NR_134989.1:n.1187T>G
NR_134990.1:n.1181T>G
NR_134991.1:n.1168T>G
NR_134992.1:n.797T>G
NR_134993.1:n.931T>G
NR_134994.1:n.1203T>G
XM_017000465.1:c.979T>G	XP_016855954.1:p.Phe327Val
XR_001737005.1:n.1269T>G
NM_000778.4:c.1291T>G MANE Select	NP_000769.2:p.Phe431Val
NM_001319155.2:c.1195T>G	NP_001306084.1:p.Phe399Val
NM_001363587.2:c.997T>G	NP_001350516.1:p.Phe333Val
NR_134988.2:n.988T>G
NR_134989.2:n.1179T>G
NR_134990.2:n.1173T>G
NR_134991.2:n.1160T>G
NR_134992.2:n.789T>G
NR_134993.2:n.923T>G
NR_134994.2:n.1195T>G