Canonical Allele Identifier: CA340223163

Gene: CYP4A11

Linked Data

• MyVariant Identifiers: chr1:g.47398466C>T (hg19) ; chr1:g.46932794C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932794C>T , CM000663.2:g.46932794C>T	GRCh38
NC_000001.10:g.47398466C>T , CM000663.1:g.47398466C>T	GRCh37
NC_000001.9:g.47171053C>T	NCBI36
NG_007932.1:g.13691G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1331G>A MANE Select	ENSP00000311095.4:p.Ser444Asn
ENST00000310638.8:c.1331G>A	ENSP00000311095.4:p.Ser444Asn
ENST00000371904.8:c.1334G>A	ENSP00000360971.4:p.Ser445Asn
ENST00000371905.1:c.1331G>A	ENSP00000360972.1:p.Ser444Asn
ENST00000462347.5:c.1037G>A	ENSP00000477495.1:p.Ser346Asn
ENST00000465874.5:c.*129G>A	ENSP00000476368.1:n.*129G>A
ENST00000468629.5:c.*36G>A	ENSP00000476619.1:n.*36G>A
ENST00000474458.5:c.*36G>A	ENSP00000476988.1:n.*36G>A
ENST00000475477.5:c.*125G>A	ENSP00000476854.1:n.*125G>A
NM_000778.3:c.1331G>A	NP_000769.2:p.Ser444Asn
XM_005270539.1:c.1037G>A	XP_005270596.1:p.Ser346Asn
XM_011540826.1:c.1349G>A	XP_011539128.1:p.Ser450Asn
XM_011540827.1:c.1055G>A	XP_011539129.1:p.Ser352Asn
XM_011540828.1:c.1037G>A	XP_011539130.1:p.Ser346Asn
XR_246241.1:n.1235G>A
XR_246242.1:n.1219G>A
NM_001319155.1:c.1235G>A	NP_001306084.1:p.Ser412Asn
NM_001363587.1:c.1037G>A	NP_001350516.1:p.Ser346Asn
NR_134988.1:n.1036G>A
NR_134989.1:n.1227G>A
NR_134990.1:n.1221G>A
NR_134991.1:n.1208G>A
NR_134992.1:n.837G>A
NR_134993.1:n.971G>A
NR_134994.1:n.1243G>A
XM_017000465.1:c.1019G>A	XP_016855954.1:p.Ser340Asn
XR_001737005.1:n.1309G>A
NM_000778.4:c.1331G>A MANE Select	NP_000769.2:p.Ser444Asn
NM_001319155.2:c.1235G>A	NP_001306084.1:p.Ser412Asn
NM_001363587.2:c.1037G>A	NP_001350516.1:p.Ser346Asn
NR_134988.2:n.1028G>A
NR_134989.2:n.1219G>A
NR_134990.2:n.1213G>A
NR_134991.2:n.1200G>A
NR_134992.2:n.829G>A
NR_134993.2:n.963G>A
NR_134994.2:n.1235G>A