Canonical Allele Identifier: CA2474389908

Gene: CYP4A11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46931142_46931143delinsGC , CM000663.2:g.46931142_46931143delinsGC	GRCh38
NC_000001.10:g.47396814_47396815delinsGC , CM000663.1:g.47396814_47396815delinsGC	GRCh37
NC_000001.9:g.47169401_47169402delinsGC	NCBI36
NG_007932.1:g.15342_15343delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1365-833_1365-832delinsGC MANE Select	ENSP00000311095.4:n.1365-833_1365-832delinsGC
ENST00000310638.8:c.1365-833_1365-832delinsGC	ENSP00000311095.4:n.1365-833_1365-832delinsGC
ENST00000371904.8:c.1368-833_1368-832delinsGC	ENSP00000360971.4:n.1368-833_1368-832delinsGC
ENST00000462347.5:c.1071-833_1071-832delinsGC	ENSP00000477495.1:n.1071-833_1071-832delinsGC
ENST00000468629.5:c.*70-833_*70-832delinsGC	ENSP00000476619.1:n.*70-833_*70-832delinsGC
ENST00000474458.5:c.*70-833_*70-832delinsGC	ENSP00000476988.1:n.*70-833_*70-832delinsGC
ENST00000475477.5:c.*159-833_*159-832delinsGC	ENSP00000476854.1:n.*159-833_*159-832delinsGC
NM_000778.3:c.1365-833_1365-832delinsGC	NP_000769.2:n.1365-833_1365-832delinsGC
XM_011540826.1:c.1383-833_1383-832delinsGC	XP_011539128.1:n.1383-833_1383-832delinsGC
XM_011540827.1:c.1089-833_1089-832delinsGC	XP_011539129.1:n.1089-833_1089-832delinsGC
XM_011540828.1:c.1071-833_1071-832delinsGC	XP_011539130.1:n.1071-833_1071-832delinsGC
XR_246241.1:n.1269-833_1269-832delinsGC
XR_246242.1:n.1253-833_1253-832delinsGC
NM_001319155.1:c.1269-833_1269-832delinsGC	NP_001306084.1:n.1269-833_1269-832delinsGC
NM_001363587.1:c.1071-833_1071-832delinsGC	NP_001350516.1:n.1071-833_1071-832delinsGC
NR_134988.1:n.1070-833_1070-832delinsGC
NR_134989.1:n.1261-833_1261-832delinsGC
NR_134990.1:n.1255-833_1255-832delinsGC
NR_134991.1:n.1242-833_1242-832delinsGC
NR_134992.1:n.871-833_871-832delinsGC
NR_134993.1:n.1005-833_1005-832delinsGC
NR_134994.1:n.1277-833_1277-832delinsGC
XM_017000465.1:c.1053-833_1053-832delinsGC	XP_016855954.1:n.1053-833_1053-832delinsGC
XR_001737005.1:n.1343-833_1343-832delinsGC
NM_000778.4:c.1365-833_1365-832delinsGC MANE Select	NP_000769.2:n.1365-833_1365-832delinsGC
NM_001319155.2:c.1269-833_1269-832delinsGC	NP_001306084.1:n.1269-833_1269-832delinsGC
NM_001363587.2:c.1071-833_1071-832delinsGC	NP_001350516.1:n.1071-833_1071-832delinsGC
NR_134988.2:n.1062-833_1062-832delinsGC
NR_134989.2:n.1253-833_1253-832delinsGC
NR_134990.2:n.1247-833_1247-832delinsGC
NR_134991.2:n.1234-833_1234-832delinsGC
NR_134992.2:n.863-833_863-832delinsGC
NR_134993.2:n.997-833_997-832delinsGC
NR_134994.2:n.1269-833_1269-832delinsGC