Canonical Allele Identifier: CA2474390831

Gene: CYP4A11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46933290_46933291delinsAG , CM000663.2:g.46933290_46933291delinsAG	GRCh38
NC_000001.10:g.47398962_47398963delinsAG , CM000663.1:g.47398962_47398963delinsAG	GRCh37
NC_000001.9:g.47171549_47171550delinsAG	NCBI36
NG_007932.1:g.13194_13195delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1223-244_1223-243delinsCT MANE Select	ENSP00000311095.4:n.1223-244_1223-243delinsCT
ENST00000310638.8:c.1223-244_1223-243delinsCT	ENSP00000311095.4:n.1223-244_1223-243delinsCT
ENST00000371904.8:c.1226-244_1226-243delinsCT	ENSP00000360971.4:n.1226-244_1226-243delinsCT
ENST00000371905.1:c.1223-244_1223-243delinsCT	ENSP00000360972.1:n.1223-244_1223-243delinsCT
ENST00000462347.5:c.929-244_929-243delinsCT	ENSP00000477495.1:n.929-244_929-243delinsCT
ENST00000465874.5:c.*21-244_*21-243delinsCT	ENSP00000476368.1:n.*21-244_*21-243delinsCT
ENST00000468629.5:c.1127-454_1127-453delinsCT	ENSP00000476619.1:n.1127-454_1127-453delinsCT
ENST00000474458.5:c.743-454_743-453delinsCT	ENSP00000476988.1:n.743-454_743-453delinsCT
ENST00000475477.5:c.*82-454_*82-453delinsCT	ENSP00000476854.1:n.*82-454_*82-453delinsCT
NM_000778.3:c.1223-244_1223-243delinsCT	NP_000769.2:n.1223-244_1223-243delinsCT
XM_005270539.1:c.929-244_929-243delinsCT	XP_005270596.1:n.929-244_929-243delinsCT
XM_011540826.1:c.1241-244_1241-243delinsCT	XP_011539128.1:n.1241-244_1241-243delinsCT
XM_011540827.1:c.947-244_947-243delinsCT	XP_011539129.1:n.947-244_947-243delinsCT
XM_011540828.1:c.929-244_929-243delinsCT	XP_011539130.1:n.929-244_929-243delinsCT
XR_246241.1:n.1127-244_1127-243delinsCT
XR_246242.1:n.1111-244_1111-243delinsCT
NM_001319155.1:c.1127-244_1127-243delinsCT	NP_001306084.1:n.1127-244_1127-243delinsCT
NM_001363587.1:c.929-244_929-243delinsCT	NP_001350516.1:n.929-244_929-243delinsCT
NR_134988.1:n.928-244_928-243delinsCT
NR_134989.1:n.1119-244_1119-243delinsCT
NR_134990.1:n.1178-454_1178-453delinsCT
NR_134991.1:n.1100-244_1100-243delinsCT
NR_134992.1:n.794-454_794-453delinsCT
NR_134993.1:n.928-454_928-453delinsCT
NR_134994.1:n.1135-244_1135-243delinsCT
XM_017000465.1:c.911-244_911-243delinsCT	XP_016855954.1:n.911-244_911-243delinsCT
XR_001737005.1:n.1266-454_1266-453delinsCT
NM_000778.4:c.1223-244_1223-243delinsCT MANE Select	NP_000769.2:n.1223-244_1223-243delinsCT
NM_001319155.2:c.1127-244_1127-243delinsCT	NP_001306084.1:n.1127-244_1127-243delinsCT
NM_001363587.2:c.929-244_929-243delinsCT	NP_001350516.1:n.929-244_929-243delinsCT
NR_134988.2:n.920-244_920-243delinsCT
NR_134989.2:n.1111-244_1111-243delinsCT
NR_134990.2:n.1170-454_1170-453delinsCT
NR_134991.2:n.1092-244_1092-243delinsCT
NR_134992.2:n.786-454_786-453delinsCT
NR_134993.2:n.920-454_920-453delinsCT
NR_134994.2:n.1127-244_1127-243delinsCT