Canonical Allele Identifier: CA340223125

Gene: CYP4A11

Linked Data

• MyVariant Identifiers: chr1:g.47398449A>C (hg19) ; chr1:g.46932777A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932777A>C , CM000663.2:g.46932777A>C	GRCh38
NC_000001.10:g.47398449A>C , CM000663.1:g.47398449A>C	GRCh37
NC_000001.9:g.47171036A>C	NCBI36
NG_007932.1:g.13708T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000310638.9:c.1348T>G MANE Select	ENSP00000311095.4:p.Phe450Val
ENST00000310638.8:c.1348T>G	ENSP00000311095.4:p.Phe450Val
ENST00000371904.8:c.1351T>G	ENSP00000360971.4:p.Phe451Val
ENST00000371905.1:c.1348T>G	ENSP00000360972.1:p.Phe450Val
ENST00000462347.5:c.1054T>G	ENSP00000477495.1:p.Phe352Val
ENST00000465874.5:c.*146T>G	ENSP00000476368.1:n.*146T>G
ENST00000468629.5:c.*53T>G	ENSP00000476619.1:n.*53T>G
ENST00000474458.5:c.*53T>G	ENSP00000476988.1:n.*53T>G
ENST00000475477.5:c.*142T>G	ENSP00000476854.1:n.*142T>G
NM_000778.3:c.1348T>G	NP_000769.2:p.Phe450Val
XM_005270539.1:c.1054T>G	XP_005270596.1:p.Phe352Val
XM_011540826.1:c.1366T>G	XP_011539128.1:p.Phe456Val
XM_011540827.1:c.1072T>G	XP_011539129.1:p.Phe358Val
XM_011540828.1:c.1054T>G	XP_011539130.1:p.Phe352Val
XR_246241.1:n.1252T>G
XR_246242.1:n.1236T>G
NM_001319155.1:c.1252T>G	NP_001306084.1:p.Phe418Val
NM_001363587.1:c.1054T>G	NP_001350516.1:p.Phe352Val
NR_134988.1:n.1053T>G
NR_134989.1:n.1244T>G
NR_134990.1:n.1238T>G
NR_134991.1:n.1225T>G
NR_134992.1:n.854T>G
NR_134993.1:n.988T>G
NR_134994.1:n.1260T>G
XM_017000465.1:c.1036T>G	XP_016855954.1:p.Phe346Val
XR_001737005.1:n.1326T>G
NM_000778.4:c.1348T>G MANE Select	NP_000769.2:p.Phe450Val
NM_001319155.2:c.1252T>G	NP_001306084.1:p.Phe418Val
NM_001363587.2:c.1054T>G	NP_001350516.1:p.Phe352Val
NR_134988.2:n.1045T>G
NR_134989.2:n.1236T>G
NR_134990.2:n.1230T>G
NR_134991.2:n.1217T>G
NR_134992.2:n.846T>G
NR_134993.2:n.980T>G
NR_134994.2:n.1252T>G