Canonical Allele Identifier: CA340223145

Gene: CYP4A11

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000310638.9:c.1339T>C MANE Select	ENSP00000311095.4:p.Phe447Leu
ENST00000310638.8:c.1339T>C	ENSP00000311095.4:p.Phe447Leu
ENST00000371904.8:c.1342T>C	ENSP00000360971.4:p.Phe448Leu
ENST00000371905.1:c.1339T>C	ENSP00000360972.1:p.Phe447Leu
ENST00000462347.5:c.1045T>C	ENSP00000477495.1:p.Phe349Leu
ENST00000465874.5:c.*137T>C	ENSP00000476368.1:n.*137T>C
ENST00000468629.5:c.*44T>C	ENSP00000476619.1:n.*44T>C
ENST00000474458.5:c.*44T>C	ENSP00000476988.1:n.*44T>C
ENST00000475477.5:c.*133T>C	ENSP00000476854.1:n.*133T>C
NM_000778.3:c.1339T>C	NP_000769.2:p.Phe447Leu
XM_005270539.1:c.1045T>C	XP_005270596.1:p.Phe349Leu
XM_011540826.1:c.1357T>C	XP_011539128.1:p.Phe453Leu
XM_011540827.1:c.1063T>C	XP_011539129.1:p.Phe355Leu
XM_011540828.1:c.1045T>C	XP_011539130.1:p.Phe349Leu
XR_246241.1:n.1243T>C
XR_246242.1:n.1227T>C
NM_001319155.1:c.1243T>C	NP_001306084.1:p.Phe415Leu
NM_001363587.1:c.1045T>C	NP_001350516.1:p.Phe349Leu
NR_134988.1:n.1044T>C
NR_134989.1:n.1235T>C
NR_134990.1:n.1229T>C
NR_134991.1:n.1216T>C
NR_134992.1:n.845T>C
NR_134993.1:n.979T>C
NR_134994.1:n.1251T>C
XM_017000465.1:c.1027T>C	XP_016855954.1:p.Phe343Leu
XR_001737005.1:n.1317T>C
NM_000778.4:c.1339T>C MANE Select	NP_000769.2:p.Phe447Leu
NM_001319155.2:c.1243T>C	NP_001306084.1:p.Phe415Leu
NM_001363587.2:c.1045T>C	NP_001350516.1:p.Phe349Leu
NR_134988.2:n.1036T>C
NR_134989.2:n.1227T>C
NR_134990.2:n.1221T>C
NR_134991.2:n.1208T>C
NR_134992.2:n.837T>C
NR_134993.2:n.971T>C
NR_134994.2:n.1243T>C