Canonical Allele Identifier: CA302990

Gene: TRMU

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.46346453A>G , CM000684.2:g.46346453A>G	GRCh38
NC_000022.10:g.46742350A>G , CM000684.1:g.46742350A>G	GRCh37
NC_000022.9:g.45121014A>G	NCBI36
NG_012173.1:g.16053A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465378.6:n.490A>G
ENST00000642562.1:c.114A>G	ENSP00000494679.1:p.Ala38=
ENST00000642923.1:c.282A>G	ENSP00000494255.1:p.Ala94=
ENST00000643137.1:c.282A>G	ENSP00000495331.1:p.Ala94=
ENST00000644006.1:c.282A>G	ENSP00000493778.1:p.Ala94=
ENST00000645026.1:n.438A>G
ENST00000645190.1:c.387A>G MANE Select	ENSP00000496496.1:p.Ala129=
ENST00000647301.1:c.387A>G	ENSP00000496641.1:p.Ala129=
ENST00000290846.8:c.387A>G	ENSP00000290846.4:p.Ala129=
ENST00000381019.3:c.387A>G	ENSP00000370407.3:p.Ala129=
ENST00000381021.7:c.280A>G	ENSP00000370409.3:p.Lys94Glu
ENST00000441818.5:c.280A>G	ENSP00000393014.1:p.Lys94Glu
ENST00000453630.5:c.280A>G	ENSP00000398488.1:p.Lys94Glu
ENST00000456595.5:c.280A>G	ENSP00000413880.1:p.Lys94Glu
ENST00000457572.5:c.387A>G	ENSP00000407700.1:p.Ala129=
ENST00000465378.5:n.519A>G
ENST00000485175.5:n.347A>G
ENST00000486620.5:n.484A>G
ENST00000496831.5:n.410A>G
NM_001282782.1:c.45A>G	NP_001269711.1:p.Ala15=
NM_001282783.1:c.26A>G	NP_001269712.1:p.Gln9Arg
NM_001282784.1:c.26A>G	NP_001269713.1:p.Gln9Arg
NM_001282785.1:c.387A>G	NP_001269714.1:p.Ala129=
NM_018006.4:c.387A>G	NP_060476.2:p.Ala129=
NR_104240.1:n.751A>G
NR_104241.1:n.644A>G
XM_005261678.1:c.50A>G	XP_005261735.1:p.Gln17Arg
XM_005261681.1:c.50A>G	XP_005261738.1:p.Gln17Arg
XM_011530271.1:c.282A>G	XP_011528573.1:p.Ala94=
XM_011530272.1:c.387A>G	XP_011528574.1:p.Ala129=
XM_011530273.1:c.387A>G	XP_011528575.1:p.Ala129=
XM_011530274.1:c.45A>G	XP_011528576.1:p.Ala15=
XM_011530275.1:c.50A>G	XP_011528577.1:p.Gln17Arg
XM_011530271.2:c.282A>G	XP_011528573.1:p.Ala94=
XM_011530272.2:c.387A>G	XP_011528574.1:p.Ala129=
XM_011530273.2:c.387A>G	XP_011528575.1:p.Ala129=
XM_011530274.2:c.45A>G	XP_011528576.1:p.Ala15=
XM_024452260.1:c.282A>G	XP_024308028.1:p.Ala94=
XR_001755261.2:n.433A>G
XR_001755262.2:n.433A>G
NM_018006.5:c.387A>G MANE Select	NP_060476.2:p.Ala129=
NM_001282782.2:c.45A>G	NP_001269711.1:p.Ala15=
NM_001282783.2:c.26A>G	NP_001269712.1:p.Gln9Arg
NM_001282784.2:c.26A>G	NP_001269713.1:p.Gln9Arg
NM_001282785.2:c.387A>G	NP_001269714.1:p.Ala129=
NR_104240.2:n.438A>G
NR_104241.2:n.331A>G