Canonical Allele Identifier: CA417756070

Gene: CYP4A11

Linked Data

• MyVariant Identifiers: chr1:g.47398706G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46933034G>T , CM000663.2:g.46933034G>T	GRCh38
NC_000001.10:g.47398706G>T , CM000663.1:g.47398706G>T	GRCh37
NC_000001.9:g.47171293G>T	NCBI36
NG_007932.1:g.13451C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1236C>A MANE Select	ENSP00000311095.4:p.Leu412=
ENST00000310638.8:c.1236C>A	ENSP00000311095.4:p.Leu412=
ENST00000371904.8:c.1239C>A	ENSP00000360971.4:p.Leu413=
ENST00000371905.1:c.1236C>A	ENSP00000360972.1:p.Leu412=
ENST00000462347.5:c.942C>A	ENSP00000477495.1:p.Leu314=
ENST00000465874.5:c.*34C>A	ENSP00000476368.1:n.*34C>A
ENST00000468629.5:c.1127-197C>A	ENSP00000476619.1:n.1127-197C>A
ENST00000474458.5:c.743-197C>A	ENSP00000476988.1:n.743-197C>A
ENST00000475477.5:c.*82-197C>A	ENSP00000476854.1:n.*82-197C>A
NM_000778.3:c.1236C>A	NP_000769.2:p.Leu412=
XM_005270539.1:c.942C>A	XP_005270596.1:p.Leu314=
XM_011540826.1:c.1254C>A	XP_011539128.1:p.Leu418=
XM_011540827.1:c.960C>A	XP_011539129.1:p.Leu320=
XM_011540828.1:c.942C>A	XP_011539130.1:p.Leu314=
XR_246241.1:n.1140C>A
XR_246242.1:n.1124C>A
NM_001319155.1:c.1140C>A	NP_001306084.1:p.Leu380=
NM_001363587.1:c.942C>A	NP_001350516.1:p.Leu314=
NR_134988.1:n.941C>A
NR_134989.1:n.1132C>A
NR_134990.1:n.1178-197C>A
NR_134991.1:n.1113C>A
NR_134992.1:n.794-197C>A
NR_134993.1:n.928-197C>A
NR_134994.1:n.1148C>A
XM_017000465.1:c.924C>A	XP_016855954.1:p.Leu308=
XR_001737005.1:n.1266-197C>A
NM_000778.4:c.1236C>A MANE Select	NP_000769.2:p.Leu412=
NM_001319155.2:c.1140C>A	NP_001306084.1:p.Leu380=
NM_001363587.2:c.942C>A	NP_001350516.1:p.Leu314=
NR_134988.2:n.933C>A
NR_134989.2:n.1124C>A
NR_134990.2:n.1170-197C>A
NR_134991.2:n.1105C>A
NR_134992.2:n.786-197C>A
NR_134993.2:n.920-197C>A
NR_134994.2:n.1140C>A