Canonical Allele Identifier: CA2474390688

Gene: CYP4A11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932974_46932975delinsAC , CM000663.2:g.46932974_46932975delinsAC	GRCh38
NC_000001.10:g.47398646_47398647delinsAC , CM000663.1:g.47398646_47398647delinsAC	GRCh37
NC_000001.9:g.47171233_47171234delinsAC	NCBI36
NG_007932.1:g.13510_13511delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1287+8_1287+9delinsGT MANE Select	ENSP00000311095.4:n.1287+8_1287+9delinsGT
ENST00000310638.8:c.1287+8_1287+9delinsGT	ENSP00000311095.4:n.1287+8_1287+9delinsGT
ENST00000371904.8:c.1290+8_1290+9delinsGT	ENSP00000360971.4:n.1290+8_1290+9delinsGT
ENST00000371905.1:c.1287+8_1287+9delinsGT	ENSP00000360972.1:n.1287+8_1287+9delinsGT
ENST00000462347.5:c.993+8_993+9delinsGT	ENSP00000477495.1:n.993+8_993+9delinsGT
ENST00000465874.5:c.*85+8_*85+9delinsGT	ENSP00000476368.1:n.*85+8_*85+9delinsGT
ENST00000468629.5:c.1127-138_1127-137delinsGT	ENSP00000476619.1:n.1127-138_1127-137delinsGT
ENST00000474458.5:c.743-138_743-137delinsGT	ENSP00000476988.1:n.743-138_743-137delinsGT
ENST00000475477.5:c.*82-138_*82-137delinsGT	ENSP00000476854.1:n.*82-138_*82-137delinsGT
NM_000778.3:c.1287+8_1287+9delinsGT	NP_000769.2:n.1287+8_1287+9delinsGT
XM_005270539.1:c.993+8_993+9delinsGT	XP_005270596.1:n.993+8_993+9delinsGT
XM_011540826.1:c.1305+8_1305+9delinsGT	XP_011539128.1:n.1305+8_1305+9delinsGT
XM_011540827.1:c.1011+8_1011+9delinsGT	XP_011539129.1:n.1011+8_1011+9delinsGT
XM_011540828.1:c.993+8_993+9delinsGT	XP_011539130.1:n.993+8_993+9delinsGT
XR_246241.1:n.1191+8_1191+9delinsGT
XR_246242.1:n.1175+8_1175+9delinsGT
NM_001319155.1:c.1191+8_1191+9delinsGT	NP_001306084.1:n.1191+8_1191+9delinsGT
NM_001363587.1:c.993+8_993+9delinsGT	NP_001350516.1:n.993+8_993+9delinsGT
NR_134988.1:n.992+8_992+9delinsGT
NR_134989.1:n.1183+8_1183+9delinsGT
NR_134990.1:n.1178-138_1178-137delinsGT
NR_134991.1:n.1164+8_1164+9delinsGT
NR_134992.1:n.794-138_794-137delinsGT
NR_134993.1:n.928-138_928-137delinsGT
NR_134994.1:n.1199+8_1199+9delinsGT
XM_017000465.1:c.975+8_975+9delinsGT	XP_016855954.1:n.975+8_975+9delinsGT
XR_001737005.1:n.1266-138_1266-137delinsGT
NM_000778.4:c.1287+8_1287+9delinsGT MANE Select	NP_000769.2:n.1287+8_1287+9delinsGT
NM_001319155.2:c.1191+8_1191+9delinsGT	NP_001306084.1:n.1191+8_1191+9delinsGT
NM_001363587.2:c.993+8_993+9delinsGT	NP_001350516.1:n.993+8_993+9delinsGT
NR_134988.2:n.984+8_984+9delinsGT
NR_134989.2:n.1175+8_1175+9delinsGT
NR_134990.2:n.1170-138_1170-137delinsGT
NR_134991.2:n.1156+8_1156+9delinsGT
NR_134992.2:n.786-138_786-137delinsGT
NR_134993.2:n.920-138_920-137delinsGT
NR_134994.2:n.1191+8_1191+9delinsGT