Canonical Allele Identifier: CA2474390399

Gene: CYP4A11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932260_46932261delinsTG , CM000663.2:g.46932260_46932261delinsTG	GRCh38
NC_000001.10:g.47397932_47397933delinsTG , CM000663.1:g.47397932_47397933delinsTG	GRCh37
NC_000001.9:g.47170519_47170520delinsTG	NCBI36
NG_007932.1:g.14224_14225delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1364+500_1364+501delinsCA MANE Select	ENSP00000311095.4:n.1364+500_1364+501delinsCA
ENST00000310638.8:c.1364+500_1364+501delinsCA	ENSP00000311095.4:n.1364+500_1364+501delinsCA
ENST00000371904.8:c.1367+500_1367+501delinsCA	ENSP00000360971.4:n.1367+500_1367+501delinsCA
ENST00000462347.5:c.1070+500_1070+501delinsCA	ENSP00000477495.1:n.1070+500_1070+501delinsCA
ENST00000465874.5:c.*662_*663delinsCA	ENSP00000476368.1:n.*662_*663delinsCA
ENST00000468629.5:c.*69+500_*69+501delinsCA	ENSP00000476619.1:n.*69+500_*69+501delinsCA
ENST00000474458.5:c.*69+500_*69+501delinsCA	ENSP00000476988.1:n.*69+500_*69+501delinsCA
ENST00000475477.5:c.*158+500_*158+501delinsCA	ENSP00000476854.1:n.*158+500_*158+501delinsCA
NM_000778.3:c.1364+500_1364+501delinsCA	NP_000769.2:n.1364+500_1364+501delinsCA
XM_011540826.1:c.1382+500_1382+501delinsCA	XP_011539128.1:n.1382+500_1382+501delinsCA
XM_011540827.1:c.1088+500_1088+501delinsCA	XP_011539129.1:n.1088+500_1088+501delinsCA
XM_011540828.1:c.1070+500_1070+501delinsCA	XP_011539130.1:n.1070+500_1070+501delinsCA
XR_246241.1:n.1268+500_1268+501delinsCA
XR_246242.1:n.1252+500_1252+501delinsCA
NM_001319155.1:c.1268+500_1268+501delinsCA	NP_001306084.1:n.1268+500_1268+501delinsCA
NM_001363587.1:c.1070+500_1070+501delinsCA	NP_001350516.1:n.1070+500_1070+501delinsCA
NR_134988.1:n.1069+500_1069+501delinsCA
NR_134989.1:n.1260+500_1260+501delinsCA
NR_134990.1:n.1254+500_1254+501delinsCA
NR_134991.1:n.1241+500_1241+501delinsCA
NR_134992.1:n.870+500_870+501delinsCA
NR_134993.1:n.1004+500_1004+501delinsCA
NR_134994.1:n.1276+500_1276+501delinsCA
XM_017000465.1:c.1052+500_1052+501delinsCA	XP_016855954.1:n.1052+500_1052+501delinsCA
XR_001737005.1:n.1342+500_1342+501delinsCA
NM_000778.4:c.1364+500_1364+501delinsCA MANE Select	NP_000769.2:n.1364+500_1364+501delinsCA
NM_001319155.2:c.1268+500_1268+501delinsCA	NP_001306084.1:n.1268+500_1268+501delinsCA
NM_001363587.2:c.1070+500_1070+501delinsCA	NP_001350516.1:n.1070+500_1070+501delinsCA
NR_134988.2:n.1061+500_1061+501delinsCA
NR_134989.2:n.1252+500_1252+501delinsCA
NR_134990.2:n.1246+500_1246+501delinsCA
NR_134991.2:n.1233+500_1233+501delinsCA
NR_134992.2:n.862+500_862+501delinsCA
NR_134993.2:n.996+500_996+501delinsCA
NR_134994.2:n.1268+500_1268+501delinsCA