Canonical Allele Identifier: CA2474390668

Gene: CYP4A11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932935_46932936delinsAT , CM000663.2:g.46932935_46932936delinsAT	GRCh38
NC_000001.10:g.47398607_47398608delinsAT , CM000663.1:g.47398607_47398608delinsAT	GRCh37
NC_000001.9:g.47171194_47171195delinsAT	NCBI36
NG_007932.1:g.13549_13550delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1287+47_1287+48delinsAT MANE Select	ENSP00000311095.4:n.1287+47_1287+48delinsAT
ENST00000310638.8:c.1287+47_1287+48delinsAT	ENSP00000311095.4:n.1287+47_1287+48delinsAT
ENST00000371904.8:c.1290+47_1290+48delinsAT	ENSP00000360971.4:n.1290+47_1290+48delinsAT
ENST00000371905.1:c.1287+47_1287+48delinsAT	ENSP00000360972.1:n.1287+47_1287+48delinsAT
ENST00000462347.5:c.993+47_993+48delinsAT	ENSP00000477495.1:n.993+47_993+48delinsAT
ENST00000465874.5:c.*85+47_*85+48delinsAT	ENSP00000476368.1:n.*85+47_*85+48delinsAT
ENST00000468629.5:c.1127-99_1127-98delinsAT	ENSP00000476619.1:n.1127-99_1127-98delinsAT
ENST00000474458.5:c.743-99_743-98delinsAT	ENSP00000476988.1:n.743-99_743-98delinsAT
ENST00000475477.5:c.*82-99_*82-98delinsAT	ENSP00000476854.1:n.*82-99_*82-98delinsAT
NM_000778.3:c.1287+47_1287+48delinsAT	NP_000769.2:n.1287+47_1287+48delinsAT
XM_005270539.1:c.993+47_993+48delinsAT	XP_005270596.1:n.993+47_993+48delinsAT
XM_011540826.1:c.1305+47_1305+48delinsAT	XP_011539128.1:n.1305+47_1305+48delinsAT
XM_011540827.1:c.1011+47_1011+48delinsAT	XP_011539129.1:n.1011+47_1011+48delinsAT
XM_011540828.1:c.993+47_993+48delinsAT	XP_011539130.1:n.993+47_993+48delinsAT
XR_246241.1:n.1191+47_1191+48delinsAT
XR_246242.1:n.1175+47_1175+48delinsAT
NM_001319155.1:c.1191+47_1191+48delinsAT	NP_001306084.1:n.1191+47_1191+48delinsAT
NM_001363587.1:c.993+47_993+48delinsAT	NP_001350516.1:n.993+47_993+48delinsAT
NR_134988.1:n.992+47_992+48delinsAT
NR_134989.1:n.1183+47_1183+48delinsAT
NR_134990.1:n.1178-99_1178-98delinsAT
NR_134991.1:n.1164+47_1164+48delinsAT
NR_134992.1:n.794-99_794-98delinsAT
NR_134993.1:n.928-99_928-98delinsAT
NR_134994.1:n.1199+47_1199+48delinsAT
XM_017000465.1:c.975+47_975+48delinsAT	XP_016855954.1:n.975+47_975+48delinsAT
XR_001737005.1:n.1266-99_1266-98delinsAT
NM_000778.4:c.1287+47_1287+48delinsAT MANE Select	NP_000769.2:n.1287+47_1287+48delinsAT
NM_001319155.2:c.1191+47_1191+48delinsAT	NP_001306084.1:n.1191+47_1191+48delinsAT
NM_001363587.2:c.993+47_993+48delinsAT	NP_001350516.1:n.993+47_993+48delinsAT
NR_134988.2:n.984+47_984+48delinsAT
NR_134989.2:n.1175+47_1175+48delinsAT
NR_134990.2:n.1170-99_1170-98delinsAT
NR_134991.2:n.1156+47_1156+48delinsAT
NR_134992.2:n.786-99_786-98delinsAT
NR_134993.2:n.920-99_920-98delinsAT
NR_134994.2:n.1191+47_1191+48delinsAT