Canonical Allele Identifier: CA2474390616

Gene: CYP4A11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932837C= , CM000663.2:g.46932837C=	GRCh38
NC_000001.10:g.47398509C= , CM000663.1:g.47398509C=	GRCh37
NC_000001.9:g.47171096C=	NCBI36
NG_007932.1:g.13648G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000310638.9:c.1288G= MANE Select	ENSP00000311095.4:p.Val430=
ENST00000310638.8:c.1288G=	ENSP00000311095.4:p.Val430=
ENST00000371904.8:c.1291G=	ENSP00000360971.4:p.Val431=
ENST00000371905.1:c.1288G=	ENSP00000360972.1:p.Val430=
ENST00000462347.5:c.994G=	ENSP00000477495.1:p.Val332=
ENST00000465874.5:c.*86G=	ENSP00000476368.1:n.*86G=
ENST00000468629.5:c.1127G=	ENSP00000476619.1:p.Gly376=
ENST00000474458.5:c.743G=	ENSP00000476988.1:p.Ser248=
ENST00000475477.5:c.*82G=	ENSP00000476854.1:n.*82G=
NM_000778.3:c.1288G=	NP_000769.2:p.Val430=
XM_005270539.1:c.994G=	XP_005270596.1:p.Val332=
XM_011540826.1:c.1306G=	XP_011539128.1:p.Val436=
XM_011540827.1:c.1012G=	XP_011539129.1:p.Val338=
XM_011540828.1:c.994G=	XP_011539130.1:p.Val332=
XR_246241.1:n.1192G=
XR_246242.1:n.1176G=
NM_001319155.1:c.1192G=	NP_001306084.1:p.Val398=
NM_001363587.1:c.994G=	NP_001350516.1:p.Val332=
NR_134988.1:n.993G=
NR_134989.1:n.1184G=
NR_134990.1:n.1178G=
NR_134991.1:n.1165G=
NR_134992.1:n.794G=
NR_134993.1:n.928G=
NR_134994.1:n.1200G=
XM_017000465.1:c.976G=	XP_016855954.1:p.Val326=
XR_001737005.1:n.1266G=
NM_000778.4:c.1288G= MANE Select	NP_000769.2:p.Val430=
NM_001319155.2:c.1192G=	NP_001306084.1:p.Val398=
NM_001363587.2:c.994G=	NP_001350516.1:p.Val332=
NR_134988.2:n.985G=
NR_134989.2:n.1176G=
NR_134990.2:n.1170G=
NR_134991.2:n.1157G=
NR_134992.2:n.786G=
NR_134993.2:n.920G=
NR_134994.2:n.1192G=