Canonical Allele Identifier: CA2408700822

Gene: TRMU

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.46352227_46352228delinsCT , CM000684.2:g.46352227_46352228delinsCT	GRCh38
NC_000022.10:g.46748124_46748125delinsCT , CM000684.1:g.46748124_46748125delinsCT	GRCh37
NC_000022.9:g.45126788_45126789delinsCT	NCBI36
NG_012173.1:g.21827_21828delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465378.6:n.754-37_754-36delinsCT
ENST00000642923.1:c.601-37_601-36delinsCT	ENSP00000494255.1:n.601-37_601-36delinsCT
ENST00000643137.1:c.601-37_601-36delinsCT	ENSP00000495331.1:n.601-37_601-36delinsCT
ENST00000644006.1:c.*150-37_*150-36delinsCT	ENSP00000493778.1:n.*150-37_*150-36delinsCT
ENST00000645026.1:n.757-37_757-36delinsCT
ENST00000645190.1:c.706-37_706-36delinsCT MANE Select	ENSP00000496496.1:n.706-37_706-36delinsCT
ENST00000647301.1:c.*150-37_*150-36delinsCT	ENSP00000496641.1:n.*150-37_*150-36delinsCT
ENST00000290846.8:c.706-37_706-36delinsCT	ENSP00000290846.4:n.706-37_706-36delinsCT
ENST00000381019.3:c.706-37_706-36delinsCT	ENSP00000370407.3:n.706-37_706-36delinsCT
ENST00000381021.7:c.*299-37_*299-36delinsCT	ENSP00000370409.3:n.*299-37_*299-36delinsCT
ENST00000441818.5:c.*240-37_*240-36delinsCT	ENSP00000393014.1:n.*240-37_*240-36delinsCT
ENST00000453630.5:c.*244-37_*244-36delinsCT	ENSP00000398488.1:n.*244-37_*244-36delinsCT
ENST00000456595.5:c.*240-37_*240-36delinsCT	ENSP00000413880.1:n.*240-37_*240-36delinsCT
ENST00000457572.5:c.*150-37_*150-36delinsCT	ENSP00000407700.1:n.*150-37_*150-36delinsCT
ENST00000463785.1:n.174-37_174-36delinsCT
ENST00000479648.1:n.526-37_526-36delinsCT
ENST00000485175.5:n.666-37_666-36delinsCT
ENST00000486620.5:n.748-37_748-36delinsCT
NM_001282782.1:c.364-37_364-36delinsCT	NP_001269711.1:n.364-37_364-36delinsCT
NM_001282783.1:c.286-37_286-36delinsCT	NP_001269712.1:n.286-37_286-36delinsCT
NM_001282784.1:c.286-37_286-36delinsCT	NP_001269713.1:n.286-37_286-36delinsCT
NM_001282785.1:c.706-37_706-36delinsCT	NP_001269714.1:n.706-37_706-36delinsCT
NM_018006.4:c.706-37_706-36delinsCT	NP_060476.2:n.706-37_706-36delinsCT
NR_104240.1:n.1015-37_1015-36delinsCT
NR_104241.1:n.908-37_908-36delinsCT
XM_005261678.1:c.310-37_310-36delinsCT	XP_005261735.1:n.310-37_310-36delinsCT
XM_005261681.1:c.310-37_310-36delinsCT	XP_005261738.1:n.310-37_310-36delinsCT
XM_011530271.1:c.601-37_601-36delinsCT	XP_011528573.1:n.601-37_601-36delinsCT
XM_011530272.1:c.706-37_706-36delinsCT	XP_011528574.1:n.706-37_706-36delinsCT
XM_011530273.1:c.706-37_706-36delinsCT	XP_011528575.1:n.706-37_706-36delinsCT
XM_011530274.1:c.364-37_364-36delinsCT	XP_011528576.1:n.364-37_364-36delinsCT
XM_011530275.1:c.310-37_310-36delinsCT	XP_011528577.1:n.310-37_310-36delinsCT
XM_011530271.2:c.601-37_601-36delinsCT	XP_011528573.1:n.601-37_601-36delinsCT
XM_011530272.2:c.706-37_706-36delinsCT	XP_011528574.1:n.706-37_706-36delinsCT
XM_011530273.2:c.706-37_706-36delinsCT	XP_011528575.1:n.706-37_706-36delinsCT
XM_011530274.2:c.364-37_364-36delinsCT	XP_011528576.1:n.364-37_364-36delinsCT
XM_024452260.1:c.601-37_601-36delinsCT	XP_024308028.1:n.601-37_601-36delinsCT
XR_001755261.2:n.752-37_752-36delinsCT
XR_001755262.2:n.752-37_752-36delinsCT
NM_018006.5:c.706-37_706-36delinsCT MANE Select	NP_060476.2:n.706-37_706-36delinsCT
NM_001282782.2:c.364-37_364-36delinsCT	NP_001269711.1:n.364-37_364-36delinsCT
NM_001282783.2:c.286-37_286-36delinsCT	NP_001269712.1:n.286-37_286-36delinsCT
NM_001282784.2:c.286-37_286-36delinsCT	NP_001269713.1:n.286-37_286-36delinsCT
NM_001282785.2:c.706-37_706-36delinsCT	NP_001269714.1:n.706-37_706-36delinsCT
NR_104240.2:n.702-37_702-36delinsCT
NR_104241.2:n.595-37_595-36delinsCT