Canonical Allele Identifier: CA2474390849

Gene: CYP4A11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46933326_46933327delinsTC , CM000663.2:g.46933326_46933327delinsTC	GRCh38
NC_000001.10:g.47398998_47398999delinsTC , CM000663.1:g.47398998_47398999delinsTC	GRCh37
NC_000001.9:g.47171585_47171586delinsTC	NCBI36
NG_007932.1:g.13158_13159delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1223-280_1223-279delinsGA MANE Select	ENSP00000311095.4:n.1223-280_1223-279delinsGA
ENST00000310638.8:c.1223-280_1223-279delinsGA	ENSP00000311095.4:n.1223-280_1223-279delinsGA
ENST00000371904.8:c.1226-280_1226-279delinsGA	ENSP00000360971.4:n.1226-280_1226-279delinsGA
ENST00000371905.1:c.1223-280_1223-279delinsGA	ENSP00000360972.1:n.1223-280_1223-279delinsGA
ENST00000462347.5:c.929-280_929-279delinsGA	ENSP00000477495.1:n.929-280_929-279delinsGA
ENST00000465874.5:c.*21-280_*21-279delinsGA	ENSP00000476368.1:n.*21-280_*21-279delinsGA
ENST00000468629.5:c.1127-490_1127-489delinsGA	ENSP00000476619.1:n.1127-490_1127-489delinsGA
ENST00000474458.5:c.743-490_743-489delinsGA	ENSP00000476988.1:n.743-490_743-489delinsGA
ENST00000475477.5:c.*82-490_*82-489delinsGA	ENSP00000476854.1:n.*82-490_*82-489delinsGA
NM_000778.3:c.1223-280_1223-279delinsGA	NP_000769.2:n.1223-280_1223-279delinsGA
XM_005270539.1:c.929-280_929-279delinsGA	XP_005270596.1:n.929-280_929-279delinsGA
XM_011540826.1:c.1241-280_1241-279delinsGA	XP_011539128.1:n.1241-280_1241-279delinsGA
XM_011540827.1:c.947-280_947-279delinsGA	XP_011539129.1:n.947-280_947-279delinsGA
XM_011540828.1:c.929-280_929-279delinsGA	XP_011539130.1:n.929-280_929-279delinsGA
XR_246241.1:n.1127-280_1127-279delinsGA
XR_246242.1:n.1111-280_1111-279delinsGA
NM_001319155.1:c.1127-280_1127-279delinsGA	NP_001306084.1:n.1127-280_1127-279delinsGA
NM_001363587.1:c.929-280_929-279delinsGA	NP_001350516.1:n.929-280_929-279delinsGA
NR_134988.1:n.928-280_928-279delinsGA
NR_134989.1:n.1119-280_1119-279delinsGA
NR_134990.1:n.1178-490_1178-489delinsGA
NR_134991.1:n.1100-280_1100-279delinsGA
NR_134992.1:n.794-490_794-489delinsGA
NR_134993.1:n.928-490_928-489delinsGA
NR_134994.1:n.1135-280_1135-279delinsGA
XM_017000465.1:c.911-280_911-279delinsGA	XP_016855954.1:n.911-280_911-279delinsGA
XR_001737005.1:n.1266-490_1266-489delinsGA
NM_000778.4:c.1223-280_1223-279delinsGA MANE Select	NP_000769.2:n.1223-280_1223-279delinsGA
NM_001319155.2:c.1127-280_1127-279delinsGA	NP_001306084.1:n.1127-280_1127-279delinsGA
NM_001363587.2:c.929-280_929-279delinsGA	NP_001350516.1:n.929-280_929-279delinsGA
NR_134988.2:n.920-280_920-279delinsGA
NR_134989.2:n.1111-280_1111-279delinsGA
NR_134990.2:n.1170-490_1170-489delinsGA
NR_134991.2:n.1092-280_1092-279delinsGA
NR_134992.2:n.786-490_786-489delinsGA
NR_134993.2:n.920-490_920-489delinsGA
NR_134994.2:n.1127-280_1127-279delinsGA