Canonical Allele Identifier: CA1148479543

Gene: CYP4A11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932936_46932937delinsTT , CM000663.2:g.46932936_46932937delinsTT	GRCh38
NC_000001.10:g.47398608_47398609delinsTT , CM000663.1:g.47398608_47398609delinsTT	GRCh37
NC_000001.9:g.47171195_47171196delinsTT	NCBI36
NG_007932.1:g.13548_13549delinsAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1287+46_1287+47delinsAA MANE Select	ENSP00000311095.4:n.1287+46_1287+47delinsAA
ENST00000310638.8:c.1287+46_1287+47delinsAA	ENSP00000311095.4:n.1287+46_1287+47delinsAA
ENST00000371904.8:c.1290+46_1290+47delinsAA	ENSP00000360971.4:n.1290+46_1290+47delinsAA
ENST00000371905.1:c.1287+46_1287+47delinsAA	ENSP00000360972.1:n.1287+46_1287+47delinsAA
ENST00000462347.5:c.993+46_993+47delinsAA	ENSP00000477495.1:n.993+46_993+47delinsAA
ENST00000465874.5:c.*85+46_*85+47delinsAA	ENSP00000476368.1:n.*85+46_*85+47delinsAA
ENST00000468629.5:c.1127-100_1127-99delinsAA	ENSP00000476619.1:n.1127-100_1127-99delinsAA
ENST00000474458.5:c.743-100_743-99delinsAA	ENSP00000476988.1:n.743-100_743-99delinsAA
ENST00000475477.5:c.*82-100_*82-99delinsAA	ENSP00000476854.1:n.*82-100_*82-99delinsAA
NM_000778.3:c.1287+46_1287+47delinsAA	NP_000769.2:n.1287+46_1287+47delinsAA
XM_005270539.1:c.993+46_993+47delinsAA	XP_005270596.1:n.993+46_993+47delinsAA
XM_011540826.1:c.1305+46_1305+47delinsAA	XP_011539128.1:n.1305+46_1305+47delinsAA
XM_011540827.1:c.1011+46_1011+47delinsAA	XP_011539129.1:n.1011+46_1011+47delinsAA
XM_011540828.1:c.993+46_993+47delinsAA	XP_011539130.1:n.993+46_993+47delinsAA
XR_246241.1:n.1191+46_1191+47delinsAA
XR_246242.1:n.1175+46_1175+47delinsAA
NM_001319155.1:c.1191+46_1191+47delinsAA	NP_001306084.1:n.1191+46_1191+47delinsAA
NM_001363587.1:c.993+46_993+47delinsAA	NP_001350516.1:n.993+46_993+47delinsAA
NR_134988.1:n.992+46_992+47delinsAA
NR_134989.1:n.1183+46_1183+47delinsAA
NR_134990.1:n.1178-100_1178-99delinsAA
NR_134991.1:n.1164+46_1164+47delinsAA
NR_134992.1:n.794-100_794-99delinsAA
NR_134993.1:n.928-100_928-99delinsAA
NR_134994.1:n.1199+46_1199+47delinsAA
XM_017000465.1:c.975+46_975+47delinsAA	XP_016855954.1:n.975+46_975+47delinsAA
XR_001737005.1:n.1266-100_1266-99delinsAA
NM_000778.4:c.1287+46_1287+47delinsAA MANE Select	NP_000769.2:n.1287+46_1287+47delinsAA
NM_001319155.2:c.1191+46_1191+47delinsAA	NP_001306084.1:n.1191+46_1191+47delinsAA
NM_001363587.2:c.993+46_993+47delinsAA	NP_001350516.1:n.993+46_993+47delinsAA
NR_134988.2:n.984+46_984+47delinsAA
NR_134989.2:n.1175+46_1175+47delinsAA
NR_134990.2:n.1170-100_1170-99delinsAA
NR_134991.2:n.1156+46_1156+47delinsAA
NR_134992.2:n.786-100_786-99delinsAA
NR_134993.2:n.920-100_920-99delinsAA
NR_134994.2:n.1191+46_1191+47delinsAA