Canonical Allele Identifier: CA2474390373

Gene: CYP4A11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932194_46932195delinsCT , CM000663.2:g.46932194_46932195delinsCT	GRCh38
NC_000001.10:g.47397866_47397867delinsCT , CM000663.1:g.47397866_47397867delinsCT	GRCh37
NC_000001.9:g.47170453_47170454delinsCT	NCBI36
NG_007932.1:g.14290_14291delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1364+566_1364+567delinsAG MANE Select	ENSP00000311095.4:n.1364+566_1364+567delinsAG
ENST00000310638.8:c.1364+566_1364+567delinsAG	ENSP00000311095.4:n.1364+566_1364+567delinsAG
ENST00000371904.8:c.1367+566_1367+567delinsAG	ENSP00000360971.4:n.1367+566_1367+567delinsAG
ENST00000462347.5:c.1070+566_1070+567delinsAG	ENSP00000477495.1:n.1070+566_1070+567delinsAG
ENST00000465874.5:c.*728_*729delinsAG	ENSP00000476368.1:n.*728_*729delinsAG
ENST00000468629.5:c.*69+566_*69+567delinsAG	ENSP00000476619.1:n.*69+566_*69+567delinsAG
ENST00000474458.5:c.*69+566_*69+567delinsAG	ENSP00000476988.1:n.*69+566_*69+567delinsAG
ENST00000475477.5:c.*158+566_*158+567delinsAG	ENSP00000476854.1:n.*158+566_*158+567delinsAG
NM_000778.3:c.1364+566_1364+567delinsAG	NP_000769.2:n.1364+566_1364+567delinsAG
XM_011540826.1:c.1382+566_1382+567delinsAG	XP_011539128.1:n.1382+566_1382+567delinsAG
XM_011540827.1:c.1088+566_1088+567delinsAG	XP_011539129.1:n.1088+566_1088+567delinsAG
XM_011540828.1:c.1070+566_1070+567delinsAG	XP_011539130.1:n.1070+566_1070+567delinsAG
XR_246241.1:n.1268+566_1268+567delinsAG
XR_246242.1:n.1252+566_1252+567delinsAG
NM_001319155.1:c.1268+566_1268+567delinsAG	NP_001306084.1:n.1268+566_1268+567delinsAG
NM_001363587.1:c.1070+566_1070+567delinsAG	NP_001350516.1:n.1070+566_1070+567delinsAG
NR_134988.1:n.1069+566_1069+567delinsAG
NR_134989.1:n.1260+566_1260+567delinsAG
NR_134990.1:n.1254+566_1254+567delinsAG
NR_134991.1:n.1241+566_1241+567delinsAG
NR_134992.1:n.870+566_870+567delinsAG
NR_134993.1:n.1004+566_1004+567delinsAG
NR_134994.1:n.1276+566_1276+567delinsAG
XM_017000465.1:c.1052+566_1052+567delinsAG	XP_016855954.1:n.1052+566_1052+567delinsAG
XR_001737005.1:n.1342+566_1342+567delinsAG
NM_000778.4:c.1364+566_1364+567delinsAG MANE Select	NP_000769.2:n.1364+566_1364+567delinsAG
NM_001319155.2:c.1268+566_1268+567delinsAG	NP_001306084.1:n.1268+566_1268+567delinsAG
NM_001363587.2:c.1070+566_1070+567delinsAG	NP_001350516.1:n.1070+566_1070+567delinsAG
NR_134988.2:n.1061+566_1061+567delinsAG
NR_134989.2:n.1252+566_1252+567delinsAG
NR_134990.2:n.1246+566_1246+567delinsAG
NR_134991.2:n.1233+566_1233+567delinsAG
NR_134992.2:n.862+566_862+567delinsAG
NR_134993.2:n.996+566_996+567delinsAG
NR_134994.2:n.1268+566_1268+567delinsAG