Canonical Allele Identifier: CA411946509

Gene: TRMU

Linked Data

• MyVariant Identifiers: chr22:g.46748206A>G (hg19) ; chr22:g.46352309A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.46352309A>G , CM000684.2:g.46352309A>G	GRCh38
NC_000022.10:g.46748206A>G , CM000684.1:g.46748206A>G	GRCh37
NC_000022.9:g.45126870A>G	NCBI36
NG_012173.1:g.21909A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465378.6:n.799A>G
ENST00000642923.1:c.646A>G	ENSP00000494255.1:p.Lys216Glu
ENST00000643137.1:c.646A>G	ENSP00000495331.1:p.Lys216Glu
ENST00000644006.1:c.*195A>G	ENSP00000493778.1:n.*195A>G
ENST00000645026.1:n.802A>G
ENST00000645190.1:c.751A>G MANE Select	ENSP00000496496.1:p.Lys251Glu
ENST00000647301.1:c.*195A>G	ENSP00000496641.1:n.*195A>G
ENST00000290846.8:c.751A>G	ENSP00000290846.4:p.Lys251Glu
ENST00000381019.3:c.751A>G	ENSP00000370407.3:p.Lys251Glu
ENST00000381021.7:c.*344A>G	ENSP00000370409.3:n.*344A>G
ENST00000441818.5:c.*285A>G	ENSP00000393014.1:n.*285A>G
ENST00000453630.5:c.*289A>G	ENSP00000398488.1:n.*289A>G
ENST00000456595.5:c.*285A>G	ENSP00000413880.1:n.*285A>G
ENST00000457572.5:c.*195A>G	ENSP00000407700.1:n.*195A>G
ENST00000463785.1:n.219A>G
ENST00000479648.1:n.571A>G
ENST00000485175.5:n.711A>G
ENST00000486620.5:n.793A>G
NM_001282782.1:c.409A>G	NP_001269711.1:p.Lys137Glu
NM_001282783.1:c.331A>G	NP_001269712.1:p.Lys111Glu
NM_001282784.1:c.331A>G	NP_001269713.1:p.Lys111Glu
NM_001282785.1:c.751A>G	NP_001269714.1:p.Lys251Glu
NM_018006.4:c.751A>G	NP_060476.2:p.Lys251Glu
NR_104240.1:n.1060A>G
NR_104241.1:n.953A>G
XM_005261678.1:c.355A>G	XP_005261735.1:p.Lys119Glu
XM_005261681.1:c.355A>G	XP_005261738.1:p.Lys119Glu
XM_011530271.1:c.646A>G	XP_011528573.1:p.Lys216Glu
XM_011530272.1:c.751A>G	XP_011528574.1:p.Lys251Glu
XM_011530273.1:c.751A>G	XP_011528575.1:p.Lys251Glu
XM_011530274.1:c.409A>G	XP_011528576.1:p.Lys137Glu
XM_011530275.1:c.355A>G	XP_011528577.1:p.Lys119Glu
XM_011530271.2:c.646A>G	XP_011528573.1:p.Lys216Glu
XM_011530272.2:c.751A>G	XP_011528574.1:p.Lys251Glu
XM_011530273.2:c.751A>G	XP_011528575.1:p.Lys251Glu
XM_011530274.2:c.409A>G	XP_011528576.1:p.Lys137Glu
XM_024452260.1:c.646A>G	XP_024308028.1:p.Lys216Glu
XR_001755261.2:n.797A>G
XR_001755262.2:n.797A>G
NM_018006.5:c.751A>G MANE Select	NP_060476.2:p.Lys251Glu
NM_001282782.2:c.409A>G	NP_001269711.1:p.Lys137Glu
NM_001282783.2:c.331A>G	NP_001269712.1:p.Lys111Glu
NM_001282784.2:c.331A>G	NP_001269713.1:p.Lys111Glu
NM_001282785.2:c.751A>G	NP_001269714.1:p.Lys251Glu
NR_104240.2:n.747A>G
NR_104241.2:n.640A>G