Canonical Allele Identifier: CA2408700868

Gene: TRMU

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.46352282G= , CM000684.2:g.46352282G=	GRCh38
NC_000022.10:g.46748179G= , CM000684.1:g.46748179G=	GRCh37
NC_000022.9:g.45126843G=	NCBI36
NG_012173.1:g.21882G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465378.6:n.772G=
ENST00000642923.1:c.619G=	ENSP00000494255.1:p.Gly207=
ENST00000643137.1:c.619G=	ENSP00000495331.1:p.Gly207=
ENST00000644006.1:c.*168G=	ENSP00000493778.1:n.*168G=
ENST00000645026.1:n.775G=
ENST00000645190.1:c.724G= MANE Select	ENSP00000496496.1:p.Gly242=
ENST00000647301.1:c.*168G=	ENSP00000496641.1:n.*168G=
ENST00000290846.8:c.724G=	ENSP00000290846.4:p.Gly242=
ENST00000381019.3:c.724G=	ENSP00000370407.3:p.Gly242=
ENST00000381021.7:c.*317G=	ENSP00000370409.3:n.*317G=
ENST00000441818.5:c.*258G=	ENSP00000393014.1:n.*258G=
ENST00000453630.5:c.*262G=	ENSP00000398488.1:n.*262G=
ENST00000456595.5:c.*258G=	ENSP00000413880.1:n.*258G=
ENST00000457572.5:c.*168G=	ENSP00000407700.1:n.*168G=
ENST00000463785.1:n.192G=
ENST00000479648.1:n.544G=
ENST00000485175.5:n.684G=
ENST00000486620.5:n.766G=
NM_001282782.1:c.382G=	NP_001269711.1:p.Gly128=
NM_001282783.1:c.304G=	NP_001269712.1:p.Gly102=
NM_001282784.1:c.304G=	NP_001269713.1:p.Gly102=
NM_001282785.1:c.724G=	NP_001269714.1:p.Gly242=
NM_018006.4:c.724G=	NP_060476.2:p.Gly242=
NR_104240.1:n.1033G=
NR_104241.1:n.926G=
XM_005261678.1:c.328G=	XP_005261735.1:p.Gly110=
XM_005261681.1:c.328G=	XP_005261738.1:p.Gly110=
XM_011530271.1:c.619G=	XP_011528573.1:p.Gly207=
XM_011530272.1:c.724G=	XP_011528574.1:p.Gly242=
XM_011530273.1:c.724G=	XP_011528575.1:p.Gly242=
XM_011530274.1:c.382G=	XP_011528576.1:p.Gly128=
XM_011530275.1:c.328G=	XP_011528577.1:p.Gly110=
XM_011530271.2:c.619G=	XP_011528573.1:p.Gly207=
XM_011530272.2:c.724G=	XP_011528574.1:p.Gly242=
XM_011530273.2:c.724G=	XP_011528575.1:p.Gly242=
XM_011530274.2:c.382G=	XP_011528576.1:p.Gly128=
XM_024452260.1:c.619G=	XP_024308028.1:p.Gly207=
XR_001755261.2:n.770G=
XR_001755262.2:n.770G=
NM_018006.5:c.724G= MANE Select	NP_060476.2:p.Gly242=
NM_001282782.2:c.382G=	NP_001269711.1:p.Gly128=
NM_001282783.2:c.304G=	NP_001269712.1:p.Gly102=
NM_001282784.2:c.304G=	NP_001269713.1:p.Gly102=
NM_001282785.2:c.724G=	NP_001269714.1:p.Gly242=
NR_104240.2:n.720G=
NR_104241.2:n.613G=