Canonical Allele Identifier: CA1145681941

Gene: CYP4A11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932335G= , CM000663.2:g.46932335G=	GRCh38
NC_000001.10:g.47398007G= , CM000663.1:g.47398007G=	GRCh37
NC_000001.9:g.47170594G=	NCBI36
NG_007932.1:g.14150C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1364+426C= MANE Select	ENSP00000311095.4:n.1364+426C=
ENST00000310638.8:c.1364+426C=	ENSP00000311095.4:n.1364+426C=
ENST00000371904.8:c.1367+426C=	ENSP00000360971.4:n.1367+426C=
ENST00000462347.5:c.1070+426C=	ENSP00000477495.1:n.1070+426C=
ENST00000465874.5:c.*588C=	ENSP00000476368.1:n.*588C=
ENST00000468629.5:c.*69+426C=	ENSP00000476619.1:n.*69+426C=
ENST00000474458.5:c.*69+426C=	ENSP00000476988.1:n.*69+426C=
ENST00000475477.5:c.*158+426C=	ENSP00000476854.1:n.*158+426C=
NM_000778.3:c.1364+426C=	NP_000769.2:n.1364+426C=
XM_011540826.1:c.1382+426C=	XP_011539128.1:n.1382+426C=
XM_011540827.1:c.1088+426C=	XP_011539129.1:n.1088+426C=
XM_011540828.1:c.1070+426C=	XP_011539130.1:n.1070+426C=
XR_246241.1:n.1268+426C=
XR_246242.1:n.1252+426C=
NM_001319155.1:c.1268+426C=	NP_001306084.1:n.1268+426C=
NM_001363587.1:c.1070+426C=	NP_001350516.1:n.1070+426C=
NR_134988.1:n.1069+426C=
NR_134989.1:n.1260+426C=
NR_134990.1:n.1254+426C=
NR_134991.1:n.1241+426C=
NR_134992.1:n.870+426C=
NR_134993.1:n.1004+426C=
NR_134994.1:n.1276+426C=
XM_017000465.1:c.1052+426C=	XP_016855954.1:n.1052+426C=
XR_001737005.1:n.1342+426C=
NM_000778.4:c.1364+426C= MANE Select	NP_000769.2:n.1364+426C=
NM_001319155.2:c.1268+426C=	NP_001306084.1:n.1268+426C=
NM_001363587.2:c.1070+426C=	NP_001350516.1:n.1070+426C=
NR_134988.2:n.1061+426C=
NR_134989.2:n.1252+426C=
NR_134990.2:n.1246+426C=
NR_134991.2:n.1233+426C=
NR_134992.2:n.862+426C=
NR_134993.2:n.996+426C=
NR_134994.2:n.1268+426C=