Canonical Allele Identifier: CA340223225

Gene: CYP4A11

Linked Data

• MyVariant Identifiers: chr1:g.47398497A>G (hg19) ; chr1:g.46932825A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932825A>G , CM000663.2:g.46932825A>G	GRCh38
NC_000001.10:g.47398497A>G , CM000663.1:g.47398497A>G	GRCh37
NC_000001.9:g.47171084A>G	NCBI36
NG_007932.1:g.13660T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000310638.9:c.1300T>C MANE Select	ENSP00000311095.4:p.Phe434Leu
ENST00000310638.8:c.1300T>C	ENSP00000311095.4:p.Phe434Leu
ENST00000371904.8:c.1303T>C	ENSP00000360971.4:p.Phe435Leu
ENST00000371905.1:c.1300T>C	ENSP00000360972.1:p.Phe434Leu
ENST00000462347.5:c.1006T>C	ENSP00000477495.1:p.Phe336Leu
ENST00000465874.5:c.*98T>C	ENSP00000476368.1:n.*98T>C
ENST00000468629.5:c.*5T>C	ENSP00000476619.1:n.*5T>C
ENST00000474458.5:c.*5T>C	ENSP00000476988.1:n.*5T>C
ENST00000475477.5:c.*94T>C	ENSP00000476854.1:n.*94T>C
NM_000778.3:c.1300T>C	NP_000769.2:p.Phe434Leu
XM_005270539.1:c.1006T>C	XP_005270596.1:p.Phe336Leu
XM_011540826.1:c.1318T>C	XP_011539128.1:p.Phe440Leu
XM_011540827.1:c.1024T>C	XP_011539129.1:p.Phe342Leu
XM_011540828.1:c.1006T>C	XP_011539130.1:p.Phe336Leu
XR_246241.1:n.1204T>C
XR_246242.1:n.1188T>C
NM_001319155.1:c.1204T>C	NP_001306084.1:p.Phe402Leu
NM_001363587.1:c.1006T>C	NP_001350516.1:p.Phe336Leu
NR_134988.1:n.1005T>C
NR_134989.1:n.1196T>C
NR_134990.1:n.1190T>C
NR_134991.1:n.1177T>C
NR_134992.1:n.806T>C
NR_134993.1:n.940T>C
NR_134994.1:n.1212T>C
XM_017000465.1:c.988T>C	XP_016855954.1:p.Phe330Leu
XR_001737005.1:n.1278T>C
NM_000778.4:c.1300T>C MANE Select	NP_000769.2:p.Phe434Leu
NM_001319155.2:c.1204T>C	NP_001306084.1:p.Phe402Leu
NM_001363587.2:c.1006T>C	NP_001350516.1:p.Phe336Leu
NR_134988.2:n.997T>C
NR_134989.2:n.1188T>C
NR_134990.2:n.1182T>C
NR_134991.2:n.1169T>C
NR_134992.2:n.798T>C
NR_134993.2:n.932T>C
NR_134994.2:n.1204T>C