Canonical Allele Identifier: CA2474390753

Gene: CYP4A11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46933126_46933127delinsAG , CM000663.2:g.46933126_46933127delinsAG	GRCh38
NC_000001.10:g.47398798_47398799delinsAG , CM000663.1:g.47398798_47398799delinsAG	GRCh37
NC_000001.9:g.47171385_47171386delinsAG	NCBI36
NG_007932.1:g.13358_13359delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1223-80_1223-79delinsCT MANE Select	ENSP00000311095.4:n.1223-80_1223-79delinsCT
ENST00000310638.8:c.1223-80_1223-79delinsCT	ENSP00000311095.4:n.1223-80_1223-79delinsCT
ENST00000371904.8:c.1226-80_1226-79delinsCT	ENSP00000360971.4:n.1226-80_1226-79delinsCT
ENST00000371905.1:c.1223-80_1223-79delinsCT	ENSP00000360972.1:n.1223-80_1223-79delinsCT
ENST00000462347.5:c.929-80_929-79delinsCT	ENSP00000477495.1:n.929-80_929-79delinsCT
ENST00000465874.5:c.*21-80_*21-79delinsCT	ENSP00000476368.1:n.*21-80_*21-79delinsCT
ENST00000468629.5:c.1127-290_1127-289delinsCT	ENSP00000476619.1:n.1127-290_1127-289delinsCT
ENST00000474458.5:c.743-290_743-289delinsCT	ENSP00000476988.1:n.743-290_743-289delinsCT
ENST00000475477.5:c.*82-290_*82-289delinsCT	ENSP00000476854.1:n.*82-290_*82-289delinsCT
NM_000778.3:c.1223-80_1223-79delinsCT	NP_000769.2:n.1223-80_1223-79delinsCT
XM_005270539.1:c.929-80_929-79delinsCT	XP_005270596.1:n.929-80_929-79delinsCT
XM_011540826.1:c.1241-80_1241-79delinsCT	XP_011539128.1:n.1241-80_1241-79delinsCT
XM_011540827.1:c.947-80_947-79delinsCT	XP_011539129.1:n.947-80_947-79delinsCT
XM_011540828.1:c.929-80_929-79delinsCT	XP_011539130.1:n.929-80_929-79delinsCT
XR_246241.1:n.1127-80_1127-79delinsCT
XR_246242.1:n.1111-80_1111-79delinsCT
NM_001319155.1:c.1127-80_1127-79delinsCT	NP_001306084.1:n.1127-80_1127-79delinsCT
NM_001363587.1:c.929-80_929-79delinsCT	NP_001350516.1:n.929-80_929-79delinsCT
NR_134988.1:n.928-80_928-79delinsCT
NR_134989.1:n.1119-80_1119-79delinsCT
NR_134990.1:n.1178-290_1178-289delinsCT
NR_134991.1:n.1100-80_1100-79delinsCT
NR_134992.1:n.794-290_794-289delinsCT
NR_134993.1:n.928-290_928-289delinsCT
NR_134994.1:n.1135-80_1135-79delinsCT
XM_017000465.1:c.911-80_911-79delinsCT	XP_016855954.1:n.911-80_911-79delinsCT
XR_001737005.1:n.1266-290_1266-289delinsCT
NM_000778.4:c.1223-80_1223-79delinsCT MANE Select	NP_000769.2:n.1223-80_1223-79delinsCT
NM_001319155.2:c.1127-80_1127-79delinsCT	NP_001306084.1:n.1127-80_1127-79delinsCT
NM_001363587.2:c.929-80_929-79delinsCT	NP_001350516.1:n.929-80_929-79delinsCT
NR_134988.2:n.920-80_920-79delinsCT
NR_134989.2:n.1111-80_1111-79delinsCT
NR_134990.2:n.1170-290_1170-289delinsCT
NR_134991.2:n.1092-80_1092-79delinsCT
NR_134992.2:n.786-290_786-289delinsCT
NR_134993.2:n.920-290_920-289delinsCT
NR_134994.2:n.1127-80_1127-79delinsCT