Canonical Allele Identifier: CA2408700816

Gene: TRMU

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.46352225_46352226delinsGC , CM000684.2:g.46352225_46352226delinsGC	GRCh38
NC_000022.10:g.46748122_46748123delinsGC , CM000684.1:g.46748122_46748123delinsGC	GRCh37
NC_000022.9:g.45126786_45126787delinsGC	NCBI36
NG_012173.1:g.21825_21826delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465378.6:n.754-39_754-38delinsGC
ENST00000642923.1:c.601-39_601-38delinsGC	ENSP00000494255.1:n.601-39_601-38delinsGC
ENST00000643137.1:c.601-39_601-38delinsGC	ENSP00000495331.1:n.601-39_601-38delinsGC
ENST00000644006.1:c.*150-39_*150-38delinsGC	ENSP00000493778.1:n.*150-39_*150-38delinsGC
ENST00000645026.1:n.757-39_757-38delinsGC
ENST00000645190.1:c.706-39_706-38delinsGC MANE Select	ENSP00000496496.1:n.706-39_706-38delinsGC
ENST00000647301.1:c.*150-39_*150-38delinsGC	ENSP00000496641.1:n.*150-39_*150-38delinsGC
ENST00000290846.8:c.706-39_706-38delinsGC	ENSP00000290846.4:n.706-39_706-38delinsGC
ENST00000381019.3:c.706-39_706-38delinsGC	ENSP00000370407.3:n.706-39_706-38delinsGC
ENST00000381021.7:c.*299-39_*299-38delinsGC	ENSP00000370409.3:n.*299-39_*299-38delinsGC
ENST00000441818.5:c.*240-39_*240-38delinsGC	ENSP00000393014.1:n.*240-39_*240-38delinsGC
ENST00000453630.5:c.*244-39_*244-38delinsGC	ENSP00000398488.1:n.*244-39_*244-38delinsGC
ENST00000456595.5:c.*240-39_*240-38delinsGC	ENSP00000413880.1:n.*240-39_*240-38delinsGC
ENST00000457572.5:c.*150-39_*150-38delinsGC	ENSP00000407700.1:n.*150-39_*150-38delinsGC
ENST00000463785.1:n.174-39_174-38delinsGC
ENST00000479648.1:n.526-39_526-38delinsGC
ENST00000485175.5:n.666-39_666-38delinsGC
ENST00000486620.5:n.748-39_748-38delinsGC
NM_001282782.1:c.364-39_364-38delinsGC	NP_001269711.1:n.364-39_364-38delinsGC
NM_001282783.1:c.286-39_286-38delinsGC	NP_001269712.1:n.286-39_286-38delinsGC
NM_001282784.1:c.286-39_286-38delinsGC	NP_001269713.1:n.286-39_286-38delinsGC
NM_001282785.1:c.706-39_706-38delinsGC	NP_001269714.1:n.706-39_706-38delinsGC
NM_018006.4:c.706-39_706-38delinsGC	NP_060476.2:n.706-39_706-38delinsGC
NR_104240.1:n.1015-39_1015-38delinsGC
NR_104241.1:n.908-39_908-38delinsGC
XM_005261678.1:c.310-39_310-38delinsGC	XP_005261735.1:n.310-39_310-38delinsGC
XM_005261681.1:c.310-39_310-38delinsGC	XP_005261738.1:n.310-39_310-38delinsGC
XM_011530271.1:c.601-39_601-38delinsGC	XP_011528573.1:n.601-39_601-38delinsGC
XM_011530272.1:c.706-39_706-38delinsGC	XP_011528574.1:n.706-39_706-38delinsGC
XM_011530273.1:c.706-39_706-38delinsGC	XP_011528575.1:n.706-39_706-38delinsGC
XM_011530274.1:c.364-39_364-38delinsGC	XP_011528576.1:n.364-39_364-38delinsGC
XM_011530275.1:c.310-39_310-38delinsGC	XP_011528577.1:n.310-39_310-38delinsGC
XM_011530271.2:c.601-39_601-38delinsGC	XP_011528573.1:n.601-39_601-38delinsGC
XM_011530272.2:c.706-39_706-38delinsGC	XP_011528574.1:n.706-39_706-38delinsGC
XM_011530273.2:c.706-39_706-38delinsGC	XP_011528575.1:n.706-39_706-38delinsGC
XM_011530274.2:c.364-39_364-38delinsGC	XP_011528576.1:n.364-39_364-38delinsGC
XM_024452260.1:c.601-39_601-38delinsGC	XP_024308028.1:n.601-39_601-38delinsGC
XR_001755261.2:n.752-39_752-38delinsGC
XR_001755262.2:n.752-39_752-38delinsGC
NM_018006.5:c.706-39_706-38delinsGC MANE Select	NP_060476.2:n.706-39_706-38delinsGC
NM_001282782.2:c.364-39_364-38delinsGC	NP_001269711.1:n.364-39_364-38delinsGC
NM_001282783.2:c.286-39_286-38delinsGC	NP_001269712.1:n.286-39_286-38delinsGC
NM_001282784.2:c.286-39_286-38delinsGC	NP_001269713.1:n.286-39_286-38delinsGC
NM_001282785.2:c.706-39_706-38delinsGC	NP_001269714.1:n.706-39_706-38delinsGC
NR_104240.2:n.702-39_702-38delinsGC
NR_104241.2:n.595-39_595-38delinsGC