Canonical Allele Identifier: CA340223091

Gene: CYP4A11

Linked Data

• dbSNP Id: rs1211676821
• gnomAD v3: 1-46932760-C-T
• gnomAD v4: 1-46932760-C-T
• MyVariant Identifiers: chr1:g.47398432C>T (hg19) ; chr1:g.46932760C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932760C>T , CM000663.2:g.46932760C>T	GRCh38
NC_000001.10:g.47398432C>T , CM000663.1:g.47398432C>T	GRCh37
NC_000001.9:g.47171019C>T	NCBI36
NG_007932.1:g.13725G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000310638.9:c.1364+1G>A MANE Select	ENSP00000311095.4:n.1364+1G>A
ENST00000310638.8:c.1364+1G>A	ENSP00000311095.4:n.1364+1G>A
ENST00000371904.8:c.1367+1G>A	ENSP00000360971.4:n.1367+1G>A
ENST00000371905.1:c.1365G>A	ENSP00000360972.1:p.Arg455=
ENST00000462347.5:c.1070+1G>A	ENSP00000477495.1:n.1070+1G>A
ENST00000465874.5:c.*163G>A	ENSP00000476368.1:n.*163G>A
ENST00000468629.5:c.*69+1G>A	ENSP00000476619.1:n.*69+1G>A
ENST00000474458.5:c.*69+1G>A	ENSP00000476988.1:n.*69+1G>A
ENST00000475477.5:c.*158+1G>A	ENSP00000476854.1:n.*158+1G>A
NM_000778.3:c.1364+1G>A	NP_000769.2:n.1364+1G>A
XM_005270539.1:c.1071G>A	XP_005270596.1:p.Arg357=
XM_011540826.1:c.1382+1G>A	XP_011539128.1:n.1382+1G>A
XM_011540827.1:c.1088+1G>A	XP_011539129.1:n.1088+1G>A
XM_011540828.1:c.1070+1G>A	XP_011539130.1:n.1070+1G>A
XR_246241.1:n.1268+1G>A
XR_246242.1:n.1252+1G>A
NM_001319155.1:c.1268+1G>A	NP_001306084.1:n.1268+1G>A
NM_001363587.1:c.1070+1G>A	NP_001350516.1:n.1070+1G>A
NR_134988.1:n.1069+1G>A
NR_134989.1:n.1260+1G>A
NR_134990.1:n.1254+1G>A
NR_134991.1:n.1241+1G>A
NR_134992.1:n.870+1G>A
NR_134993.1:n.1004+1G>A
NR_134994.1:n.1276+1G>A
XM_017000465.1:c.1052+1G>A	XP_016855954.1:n.1052+1G>A
XR_001737005.1:n.1342+1G>A
NM_000778.4:c.1364+1G>A MANE Select	NP_000769.2:n.1364+1G>A
NM_001319155.2:c.1268+1G>A	NP_001306084.1:n.1268+1G>A
NM_001363587.2:c.1070+1G>A	NP_001350516.1:n.1070+1G>A
NR_134988.2:n.1061+1G>A
NR_134989.2:n.1252+1G>A
NR_134990.2:n.1246+1G>A
NR_134991.2:n.1233+1G>A
NR_134992.2:n.862+1G>A
NR_134993.2:n.996+1G>A
NR_134994.2:n.1268+1G>A