Canonical Allele Identifier: CA340223143

Gene: CYP4A11

Linked Data

• MyVariant Identifiers: chr1:g.47398458A>C (hg19) ; chr1:g.46932786A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932786A>C , CM000663.2:g.46932786A>C	GRCh38
NC_000001.10:g.47398458A>C , CM000663.1:g.47398458A>C	GRCh37
NC_000001.9:g.47171045A>C	NCBI36
NG_007932.1:g.13699T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000310638.9:c.1339T>G MANE Select	ENSP00000311095.4:p.Phe447Val
ENST00000310638.8:c.1339T>G	ENSP00000311095.4:p.Phe447Val
ENST00000371904.8:c.1342T>G	ENSP00000360971.4:p.Phe448Val
ENST00000371905.1:c.1339T>G	ENSP00000360972.1:p.Phe447Val
ENST00000462347.5:c.1045T>G	ENSP00000477495.1:p.Phe349Val
ENST00000465874.5:c.*137T>G	ENSP00000476368.1:n.*137T>G
ENST00000468629.5:c.*44T>G	ENSP00000476619.1:n.*44T>G
ENST00000474458.5:c.*44T>G	ENSP00000476988.1:n.*44T>G
ENST00000475477.5:c.*133T>G	ENSP00000476854.1:n.*133T>G
NM_000778.3:c.1339T>G	NP_000769.2:p.Phe447Val
XM_005270539.1:c.1045T>G	XP_005270596.1:p.Phe349Val
XM_011540826.1:c.1357T>G	XP_011539128.1:p.Phe453Val
XM_011540827.1:c.1063T>G	XP_011539129.1:p.Phe355Val
XM_011540828.1:c.1045T>G	XP_011539130.1:p.Phe349Val
XR_246241.1:n.1243T>G
XR_246242.1:n.1227T>G
NM_001319155.1:c.1243T>G	NP_001306084.1:p.Phe415Val
NM_001363587.1:c.1045T>G	NP_001350516.1:p.Phe349Val
NR_134988.1:n.1044T>G
NR_134989.1:n.1235T>G
NR_134990.1:n.1229T>G
NR_134991.1:n.1216T>G
NR_134992.1:n.845T>G
NR_134993.1:n.979T>G
NR_134994.1:n.1251T>G
XM_017000465.1:c.1027T>G	XP_016855954.1:p.Phe343Val
XR_001737005.1:n.1317T>G
NM_000778.4:c.1339T>G MANE Select	NP_000769.2:p.Phe447Val
NM_001319155.2:c.1243T>G	NP_001306084.1:p.Phe415Val
NM_001363587.2:c.1045T>G	NP_001350516.1:p.Phe349Val
NR_134988.2:n.1036T>G
NR_134989.2:n.1227T>G
NR_134990.2:n.1221T>G
NR_134991.2:n.1208T>G
NR_134992.2:n.837T>G
NR_134993.2:n.971T>G
NR_134994.2:n.1243T>G