Canonical Allele Identifier: CA1146230816

Gene: CYP4A11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46933302_46933304delinsGTG , CM000663.2:g.46933302_46933304delinsGTG	GRCh38
NC_000001.10:g.47398974_47398976delinsGTG , CM000663.1:g.47398974_47398976delinsGTG	GRCh37
NC_000001.9:g.47171561_47171563delinsGTG	NCBI36
NG_007932.1:g.13181_13183delinsCAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1223-257_1223-255delinsCAC MANE Select	ENSP00000311095.4:n.1223-257_1223-255delinsCAC
ENST00000310638.8:c.1223-257_1223-255delinsCAC	ENSP00000311095.4:n.1223-257_1223-255delinsCAC
ENST00000371904.8:c.1226-257_1226-255delinsCAC	ENSP00000360971.4:n.1226-257_1226-255delinsCAC
ENST00000371905.1:c.1223-257_1223-255delinsCAC	ENSP00000360972.1:n.1223-257_1223-255delinsCAC
ENST00000462347.5:c.929-257_929-255delinsCAC	ENSP00000477495.1:n.929-257_929-255delinsCAC
ENST00000465874.5:c.*21-257_*21-255delinsCAC	ENSP00000476368.1:n.*21-257_*21-255delinsCAC
ENST00000468629.5:c.1127-467_1127-465delinsCAC	ENSP00000476619.1:n.1127-467_1127-465delinsCAC
ENST00000474458.5:c.743-467_743-465delinsCAC	ENSP00000476988.1:n.743-467_743-465delinsCAC
ENST00000475477.5:c.*82-467_*82-465delinsCAC	ENSP00000476854.1:n.*82-467_*82-465delinsCAC
NM_000778.3:c.1223-257_1223-255delinsCAC	NP_000769.2:n.1223-257_1223-255delinsCAC
XM_005270539.1:c.929-257_929-255delinsCAC	XP_005270596.1:n.929-257_929-255delinsCAC
XM_011540826.1:c.1241-257_1241-255delinsCAC	XP_011539128.1:n.1241-257_1241-255delinsCAC
XM_011540827.1:c.947-257_947-255delinsCAC	XP_011539129.1:n.947-257_947-255delinsCAC
XM_011540828.1:c.929-257_929-255delinsCAC	XP_011539130.1:n.929-257_929-255delinsCAC
XR_246241.1:n.1127-257_1127-255delinsCAC
XR_246242.1:n.1111-257_1111-255delinsCAC
NM_001319155.1:c.1127-257_1127-255delinsCAC	NP_001306084.1:n.1127-257_1127-255delinsCAC
NM_001363587.1:c.929-257_929-255delinsCAC	NP_001350516.1:n.929-257_929-255delinsCAC
NR_134988.1:n.928-257_928-255delinsCAC
NR_134989.1:n.1119-257_1119-255delinsCAC
NR_134990.1:n.1178-467_1178-465delinsCAC
NR_134991.1:n.1100-257_1100-255delinsCAC
NR_134992.1:n.794-467_794-465delinsCAC
NR_134993.1:n.928-467_928-465delinsCAC
NR_134994.1:n.1135-257_1135-255delinsCAC
XM_017000465.1:c.911-257_911-255delinsCAC	XP_016855954.1:n.911-257_911-255delinsCAC
XR_001737005.1:n.1266-467_1266-465delinsCAC
NM_000778.4:c.1223-257_1223-255delinsCAC MANE Select	NP_000769.2:n.1223-257_1223-255delinsCAC
NM_001319155.2:c.1127-257_1127-255delinsCAC	NP_001306084.1:n.1127-257_1127-255delinsCAC
NM_001363587.2:c.929-257_929-255delinsCAC	NP_001350516.1:n.929-257_929-255delinsCAC
NR_134988.2:n.920-257_920-255delinsCAC
NR_134989.2:n.1111-257_1111-255delinsCAC
NR_134990.2:n.1170-467_1170-465delinsCAC
NR_134991.2:n.1092-257_1092-255delinsCAC
NR_134992.2:n.786-467_786-465delinsCAC
NR_134993.2:n.920-467_920-465delinsCAC
NR_134994.2:n.1127-257_1127-255delinsCAC