Canonical Allele Identifier: CA417756048

Gene: CYP4A11

Linked Data

• gnomAD v4: 1-46933004-T-A
• MyVariant Identifiers: chr1:g.47398676T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46933004T>A , CM000663.2:g.46933004T>A	GRCh38
NC_000001.10:g.47398676T>A , CM000663.1:g.47398676T>A	GRCh37
NC_000001.9:g.47171263T>A	NCBI36
NG_007932.1:g.13481A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1266A>T MANE Select	ENSP00000311095.4:p.Pro422=
ENST00000310638.8:c.1266A>T	ENSP00000311095.4:p.Pro422=
ENST00000371904.8:c.1269A>T	ENSP00000360971.4:p.Pro423=
ENST00000371905.1:c.1266A>T	ENSP00000360972.1:p.Pro422=
ENST00000462347.5:c.972A>T	ENSP00000477495.1:p.Pro324=
ENST00000465874.5:c.*64A>T	ENSP00000476368.1:n.*64A>T
ENST00000468629.5:c.1127-167A>T	ENSP00000476619.1:n.1127-167A>T
ENST00000474458.5:c.743-167A>T	ENSP00000476988.1:n.743-167A>T
ENST00000475477.5:c.*82-167A>T	ENSP00000476854.1:n.*82-167A>T
NM_000778.3:c.1266A>T	NP_000769.2:p.Pro422=
XM_005270539.1:c.972A>T	XP_005270596.1:p.Pro324=
XM_011540826.1:c.1284A>T	XP_011539128.1:p.Pro428=
XM_011540827.1:c.990A>T	XP_011539129.1:p.Pro330=
XM_011540828.1:c.972A>T	XP_011539130.1:p.Pro324=
XR_246241.1:n.1170A>T
XR_246242.1:n.1154A>T
NM_001319155.1:c.1170A>T	NP_001306084.1:p.Pro390=
NM_001363587.1:c.972A>T	NP_001350516.1:p.Pro324=
NR_134988.1:n.971A>T
NR_134989.1:n.1162A>T
NR_134990.1:n.1178-167A>T
NR_134991.1:n.1143A>T
NR_134992.1:n.794-167A>T
NR_134993.1:n.928-167A>T
NR_134994.1:n.1178A>T
XM_017000465.1:c.954A>T	XP_016855954.1:p.Pro318=
XR_001737005.1:n.1266-167A>T
NM_000778.4:c.1266A>T MANE Select	NP_000769.2:p.Pro422=
NM_001319155.2:c.1170A>T	NP_001306084.1:p.Pro390=
NM_001363587.2:c.972A>T	NP_001350516.1:p.Pro324=
NR_134988.2:n.963A>T
NR_134989.2:n.1154A>T
NR_134990.2:n.1170-167A>T
NR_134991.2:n.1135A>T
NR_134992.2:n.786-167A>T
NR_134993.2:n.920-167A>T
NR_134994.2:n.1170A>T