Canonical Allele Identifier: CA2743477729

Gene: CYP4A11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46933137_46933138insCACACCCAACAC , CM000663.2:g.46933137_46933138insCACACCCAACAC	GRCh38
NC_000001.10:g.47398809_47398810insCACACCCAACAC , CM000663.1:g.47398809_47398810insCACACCCAACAC	GRCh37
NC_000001.9:g.47171396_47171397insCACACCCAACAC	NCBI36
NG_007932.1:g.13347_13348insGTGTTGGGTGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1223-91_1223-90insGTGTTGGGTGTG MANE Select	ENSP00000311095.4:n.1223-91_1223-90insGTGTTGGGTGTG
ENST00000310638.8:c.1223-91_1223-90insGTGTTGGGTGTG	ENSP00000311095.4:n.1223-91_1223-90insGTGTTGGGTGTG
ENST00000371904.8:c.1226-91_1226-90insGTGTTGGGTGTG	ENSP00000360971.4:n.1226-91_1226-90insGTGTTGGGTGTG
ENST00000371905.1:c.1223-91_1223-90insGTGTTGGGTGTG	ENSP00000360972.1:n.1223-91_1223-90insGTGTTGGGTGTG
ENST00000462347.5:c.929-91_929-90insGTGTTGGGTGTG	ENSP00000477495.1:n.929-91_929-90insGTGTTGGGTGTG
ENST00000465874.5:c.*21-91_*21-90insGTGTTGGGTGTG	ENSP00000476368.1:n.*21-91_*21-90insGTGTTGGGTGTG
ENST00000468629.5:c.1127-301_1127-300insGTGTTGGGTGTG	ENSP00000476619.1:n.1127-301_1127-300insGTGTTGGGTGTG
ENST00000474458.5:c.743-301_743-300insGTGTTGGGTGTG	ENSP00000476988.1:n.743-301_743-300insGTGTTGGGTGTG
ENST00000475477.5:c.*82-301_*82-300insGTGTTGGGTGTG	ENSP00000476854.1:n.*82-301_*82-300insGTGTTGGGTGTG
NM_000778.3:c.1223-91_1223-90insGTGTTGGGTGTG	NP_000769.2:n.1223-91_1223-90insGTGTTGGGTGTG
XM_005270539.1:c.929-91_929-90insGTGTTGGGTGTG	XP_005270596.1:n.929-91_929-90insGTGTTGGGTGTG
XM_011540826.1:c.1241-91_1241-90insGTGTTGGGTGTG	XP_011539128.1:n.1241-91_1241-90insGTGTTGGGTGTG
XM_011540827.1:c.947-91_947-90insGTGTTGGGTGTG	XP_011539129.1:n.947-91_947-90insGTGTTGGGTGTG
XM_011540828.1:c.929-91_929-90insGTGTTGGGTGTG	XP_011539130.1:n.929-91_929-90insGTGTTGGGTGTG
XR_246241.1:n.1127-91_1127-90insGTGTTGGGTGTG
XR_246242.1:n.1111-91_1111-90insGTGTTGGGTGTG
NM_001319155.1:c.1127-91_1127-90insGTGTTGGGTGTG	NP_001306084.1:n.1127-91_1127-90insGTGTTGGGTGTG
NM_001363587.1:c.929-91_929-90insGTGTTGGGTGTG	NP_001350516.1:n.929-91_929-90insGTGTTGGGTGTG
NR_134988.1:n.928-91_928-90insGTGTTGGGTGTG
NR_134989.1:n.1119-91_1119-90insGTGTTGGGTGTG
NR_134990.1:n.1178-301_1178-300insGTGTTGGGTGTG
NR_134991.1:n.1100-91_1100-90insGTGTTGGGTGTG
NR_134992.1:n.794-301_794-300insGTGTTGGGTGTG
NR_134993.1:n.928-301_928-300insGTGTTGGGTGTG
NR_134994.1:n.1135-91_1135-90insGTGTTGGGTGTG
XM_017000465.1:c.911-91_911-90insGTGTTGGGTGTG	XP_016855954.1:n.911-91_911-90insGTGTTGGGTGTG
XR_001737005.1:n.1266-301_1266-300insGTGTTGGGTGTG
NM_000778.4:c.1223-91_1223-90insGTGTTGGGTGTG MANE Select	NP_000769.2:n.1223-91_1223-90insGTGTTGGGTGTG
NM_001319155.2:c.1127-91_1127-90insGTGTTGGGTGTG	NP_001306084.1:n.1127-91_1127-90insGTGTTGGGTGTG
NM_001363587.2:c.929-91_929-90insGTGTTGGGTGTG	NP_001350516.1:n.929-91_929-90insGTGTTGGGTGTG
NR_134988.2:n.920-91_920-90insGTGTTGGGTGTG
NR_134989.2:n.1111-91_1111-90insGTGTTGGGTGTG
NR_134990.2:n.1170-301_1170-300insGTGTTGGGTGTG
NR_134991.2:n.1092-91_1092-90insGTGTTGGGTGTG
NR_134992.2:n.786-301_786-300insGTGTTGGGTGTG
NR_134993.2:n.920-301_920-300insGTGTTGGGTGTG
NR_134994.2:n.1127-91_1127-90insGTGTTGGGTGTG