Canonical Allele Identifier: CA2474390446

Gene: CYP4A11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932364_46932365delinsGT , CM000663.2:g.46932364_46932365delinsGT	GRCh38
NC_000001.10:g.47398036_47398037delinsGT , CM000663.1:g.47398036_47398037delinsGT	GRCh37
NC_000001.9:g.47170623_47170624delinsGT	NCBI36
NG_007932.1:g.14120_14121delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1364+396_1364+397delinsAC MANE Select	ENSP00000311095.4:n.1364+396_1364+397delinsAC
ENST00000310638.8:c.1364+396_1364+397delinsAC	ENSP00000311095.4:n.1364+396_1364+397delinsAC
ENST00000371904.8:c.1367+396_1367+397delinsAC	ENSP00000360971.4:n.1367+396_1367+397delinsAC
ENST00000462347.5:c.1070+396_1070+397delinsAC	ENSP00000477495.1:n.1070+396_1070+397delinsAC
ENST00000465874.5:c.*558_*559delinsAC	ENSP00000476368.1:n.*558_*559delinsAC
ENST00000468629.5:c.*69+396_*69+397delinsAC	ENSP00000476619.1:n.*69+396_*69+397delinsAC
ENST00000474458.5:c.*69+396_*69+397delinsAC	ENSP00000476988.1:n.*69+396_*69+397delinsAC
ENST00000475477.5:c.*158+396_*158+397delinsAC	ENSP00000476854.1:n.*158+396_*158+397delinsAC
NM_000778.3:c.1364+396_1364+397delinsAC	NP_000769.2:n.1364+396_1364+397delinsAC
XM_011540826.1:c.1382+396_1382+397delinsAC	XP_011539128.1:n.1382+396_1382+397delinsAC
XM_011540827.1:c.1088+396_1088+397delinsAC	XP_011539129.1:n.1088+396_1088+397delinsAC
XM_011540828.1:c.1070+396_1070+397delinsAC	XP_011539130.1:n.1070+396_1070+397delinsAC
XR_246241.1:n.1268+396_1268+397delinsAC
XR_246242.1:n.1252+396_1252+397delinsAC
NM_001319155.1:c.1268+396_1268+397delinsAC	NP_001306084.1:n.1268+396_1268+397delinsAC
NM_001363587.1:c.1070+396_1070+397delinsAC	NP_001350516.1:n.1070+396_1070+397delinsAC
NR_134988.1:n.1069+396_1069+397delinsAC
NR_134989.1:n.1260+396_1260+397delinsAC
NR_134990.1:n.1254+396_1254+397delinsAC
NR_134991.1:n.1241+396_1241+397delinsAC
NR_134992.1:n.870+396_870+397delinsAC
NR_134993.1:n.1004+396_1004+397delinsAC
NR_134994.1:n.1276+396_1276+397delinsAC
XM_017000465.1:c.1052+396_1052+397delinsAC	XP_016855954.1:n.1052+396_1052+397delinsAC
XR_001737005.1:n.1342+396_1342+397delinsAC
NM_000778.4:c.1364+396_1364+397delinsAC MANE Select	NP_000769.2:n.1364+396_1364+397delinsAC
NM_001319155.2:c.1268+396_1268+397delinsAC	NP_001306084.1:n.1268+396_1268+397delinsAC
NM_001363587.2:c.1070+396_1070+397delinsAC	NP_001350516.1:n.1070+396_1070+397delinsAC
NR_134988.2:n.1061+396_1061+397delinsAC
NR_134989.2:n.1252+396_1252+397delinsAC
NR_134990.2:n.1246+396_1246+397delinsAC
NR_134991.2:n.1233+396_1233+397delinsAC
NR_134992.2:n.862+396_862+397delinsAC
NR_134993.2:n.996+396_996+397delinsAC
NR_134994.2:n.1268+396_1268+397delinsAC