Canonical Allele Identifier: CA2474390756

Gene: CYP4A11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46933134_46933135delinsCA , CM000663.2:g.46933134_46933135delinsCA	GRCh38
NC_000001.10:g.47398806_47398807delinsCA , CM000663.1:g.47398806_47398807delinsCA	GRCh37
NC_000001.9:g.47171393_47171394delinsCA	NCBI36
NG_007932.1:g.13350_13351delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1223-88_1223-87delinsTG MANE Select	ENSP00000311095.4:n.1223-88_1223-87delinsTG
ENST00000310638.8:c.1223-88_1223-87delinsTG	ENSP00000311095.4:n.1223-88_1223-87delinsTG
ENST00000371904.8:c.1226-88_1226-87delinsTG	ENSP00000360971.4:n.1226-88_1226-87delinsTG
ENST00000371905.1:c.1223-88_1223-87delinsTG	ENSP00000360972.1:n.1223-88_1223-87delinsTG
ENST00000462347.5:c.929-88_929-87delinsTG	ENSP00000477495.1:n.929-88_929-87delinsTG
ENST00000465874.5:c.*21-88_*21-87delinsTG	ENSP00000476368.1:n.*21-88_*21-87delinsTG
ENST00000468629.5:c.1127-298_1127-297delinsTG	ENSP00000476619.1:n.1127-298_1127-297delinsTG
ENST00000474458.5:c.743-298_743-297delinsTG	ENSP00000476988.1:n.743-298_743-297delinsTG
ENST00000475477.5:c.*82-298_*82-297delinsTG	ENSP00000476854.1:n.*82-298_*82-297delinsTG
NM_000778.3:c.1223-88_1223-87delinsTG	NP_000769.2:n.1223-88_1223-87delinsTG
XM_005270539.1:c.929-88_929-87delinsTG	XP_005270596.1:n.929-88_929-87delinsTG
XM_011540826.1:c.1241-88_1241-87delinsTG	XP_011539128.1:n.1241-88_1241-87delinsTG
XM_011540827.1:c.947-88_947-87delinsTG	XP_011539129.1:n.947-88_947-87delinsTG
XM_011540828.1:c.929-88_929-87delinsTG	XP_011539130.1:n.929-88_929-87delinsTG
XR_246241.1:n.1127-88_1127-87delinsTG
XR_246242.1:n.1111-88_1111-87delinsTG
NM_001319155.1:c.1127-88_1127-87delinsTG	NP_001306084.1:n.1127-88_1127-87delinsTG
NM_001363587.1:c.929-88_929-87delinsTG	NP_001350516.1:n.929-88_929-87delinsTG
NR_134988.1:n.928-88_928-87delinsTG
NR_134989.1:n.1119-88_1119-87delinsTG
NR_134990.1:n.1178-298_1178-297delinsTG
NR_134991.1:n.1100-88_1100-87delinsTG
NR_134992.1:n.794-298_794-297delinsTG
NR_134993.1:n.928-298_928-297delinsTG
NR_134994.1:n.1135-88_1135-87delinsTG
XM_017000465.1:c.911-88_911-87delinsTG	XP_016855954.1:n.911-88_911-87delinsTG
XR_001737005.1:n.1266-298_1266-297delinsTG
NM_000778.4:c.1223-88_1223-87delinsTG MANE Select	NP_000769.2:n.1223-88_1223-87delinsTG
NM_001319155.2:c.1127-88_1127-87delinsTG	NP_001306084.1:n.1127-88_1127-87delinsTG
NM_001363587.2:c.929-88_929-87delinsTG	NP_001350516.1:n.929-88_929-87delinsTG
NR_134988.2:n.920-88_920-87delinsTG
NR_134989.2:n.1111-88_1111-87delinsTG
NR_134990.2:n.1170-298_1170-297delinsTG
NR_134991.2:n.1092-88_1092-87delinsTG
NR_134992.2:n.786-298_786-297delinsTG
NR_134993.2:n.920-298_920-297delinsTG
NR_134994.2:n.1127-88_1127-87delinsTG