Canonical Allele Identifier: CA411946144

Gene: TRMU

Linked Data

• MyVariant Identifiers: chr22:g.46748034T>G (hg19) ; chr22:g.46352137T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.46352137T>G , CM000684.2:g.46352137T>G	GRCh38
NC_000022.10:g.46748034T>G , CM000684.1:g.46748034T>G	GRCh37
NC_000022.9:g.45126698T>G	NCBI36
NG_012173.1:g.21737T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465378.6:n.716T>G
ENST00000642923.1:c.563T>G	ENSP00000494255.1:p.Phe188Cys
ENST00000643137.1:c.563T>G	ENSP00000495331.1:p.Phe188Cys
ENST00000644006.1:c.*112T>G	ENSP00000493778.1:n.*112T>G
ENST00000645026.1:n.719T>G
ENST00000645190.1:c.668T>G MANE Select	ENSP00000496496.1:p.Phe223Cys
ENST00000647301.1:c.*112T>G	ENSP00000496641.1:n.*112T>G
ENST00000290846.8:c.668T>G	ENSP00000290846.4:p.Phe223Cys
ENST00000381019.3:c.668T>G	ENSP00000370407.3:p.Phe223Cys
ENST00000381021.7:c.*261T>G	ENSP00000370409.3:n.*261T>G
ENST00000441818.5:c.*202T>G	ENSP00000393014.1:n.*202T>G
ENST00000453630.5:c.*206T>G	ENSP00000398488.1:n.*206T>G
ENST00000456595.5:c.*202T>G	ENSP00000413880.1:n.*202T>G
ENST00000457572.5:c.*112T>G	ENSP00000407700.1:n.*112T>G
ENST00000463785.1:n.136T>G
ENST00000479648.1:n.488T>G
ENST00000485175.5:n.628T>G
ENST00000486620.5:n.710T>G
NM_001282782.1:c.326T>G	NP_001269711.1:p.Phe109Cys
NM_001282783.1:c.248T>G	NP_001269712.1:p.Phe83Cys
NM_001282784.1:c.248T>G	NP_001269713.1:p.Phe83Cys
NM_001282785.1:c.668T>G	NP_001269714.1:p.Phe223Cys
NM_018006.4:c.668T>G	NP_060476.2:p.Phe223Cys
NR_104240.1:n.977T>G
NR_104241.1:n.870T>G
XM_005261678.1:c.272T>G	XP_005261735.1:p.Phe91Cys
XM_005261681.1:c.272T>G	XP_005261738.1:p.Phe91Cys
XM_011530271.1:c.563T>G	XP_011528573.1:p.Phe188Cys
XM_011530272.1:c.668T>G	XP_011528574.1:p.Phe223Cys
XM_011530273.1:c.668T>G	XP_011528575.1:p.Phe223Cys
XM_011530274.1:c.326T>G	XP_011528576.1:p.Phe109Cys
XM_011530275.1:c.272T>G	XP_011528577.1:p.Phe91Cys
XM_011530271.2:c.563T>G	XP_011528573.1:p.Phe188Cys
XM_011530272.2:c.668T>G	XP_011528574.1:p.Phe223Cys
XM_011530273.2:c.668T>G	XP_011528575.1:p.Phe223Cys
XM_011530274.2:c.326T>G	XP_011528576.1:p.Phe109Cys
XM_024452260.1:c.563T>G	XP_024308028.1:p.Phe188Cys
XR_001755261.2:n.714T>G
XR_001755262.2:n.714T>G
NM_018006.5:c.668T>G MANE Select	NP_060476.2:p.Phe223Cys
NM_001282782.2:c.326T>G	NP_001269711.1:p.Phe109Cys
NM_001282783.2:c.248T>G	NP_001269712.1:p.Phe83Cys
NM_001282784.2:c.248T>G	NP_001269713.1:p.Phe83Cys
NM_001282785.2:c.668T>G	NP_001269714.1:p.Phe223Cys
NR_104240.2:n.664T>G
NR_104241.2:n.557T>G