Canonical Allele Identifier: CA411946125

Gene: TRMU

Linked Data

• MyVariant Identifiers: chr22:g.46748027A>G (hg19) ; chr22:g.46352130A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.46352130A>G , CM000684.2:g.46352130A>G	GRCh38
NC_000022.10:g.46748027A>G , CM000684.1:g.46748027A>G	GRCh37
NC_000022.9:g.45126691A>G	NCBI36
NG_012173.1:g.21730A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465378.6:n.709A>G
ENST00000642923.1:c.556A>G	ENSP00000494255.1:p.Met186Val
ENST00000643137.1:c.556A>G	ENSP00000495331.1:p.Met186Val
ENST00000644006.1:c.*105A>G	ENSP00000493778.1:n.*105A>G
ENST00000645026.1:n.712A>G
ENST00000645190.1:c.661A>G MANE Select	ENSP00000496496.1:p.Met221Val
ENST00000647301.1:c.*105A>G	ENSP00000496641.1:n.*105A>G
ENST00000290846.8:c.661A>G	ENSP00000290846.4:p.Met221Val
ENST00000381019.3:c.661A>G	ENSP00000370407.3:p.Met221Val
ENST00000381021.7:c.*254A>G	ENSP00000370409.3:n.*254A>G
ENST00000441818.5:c.*195A>G	ENSP00000393014.1:n.*195A>G
ENST00000453630.5:c.*199A>G	ENSP00000398488.1:n.*199A>G
ENST00000456595.5:c.*195A>G	ENSP00000413880.1:n.*195A>G
ENST00000457572.5:c.*105A>G	ENSP00000407700.1:n.*105A>G
ENST00000463785.1:n.129A>G
ENST00000479648.1:n.481A>G
ENST00000485175.5:n.621A>G
ENST00000486620.5:n.703A>G
NM_001282782.1:c.319A>G	NP_001269711.1:p.Met107Val
NM_001282783.1:c.241A>G	NP_001269712.1:p.Met81Val
NM_001282784.1:c.241A>G	NP_001269713.1:p.Met81Val
NM_001282785.1:c.661A>G	NP_001269714.1:p.Met221Val
NM_018006.4:c.661A>G	NP_060476.2:p.Met221Val
NR_104240.1:n.970A>G
NR_104241.1:n.863A>G
XM_005261678.1:c.265A>G	XP_005261735.1:p.Met89Val
XM_005261681.1:c.265A>G	XP_005261738.1:p.Met89Val
XM_011530271.1:c.556A>G	XP_011528573.1:p.Met186Val
XM_011530272.1:c.661A>G	XP_011528574.1:p.Met221Val
XM_011530273.1:c.661A>G	XP_011528575.1:p.Met221Val
XM_011530274.1:c.319A>G	XP_011528576.1:p.Met107Val
XM_011530275.1:c.265A>G	XP_011528577.1:p.Met89Val
XM_011530271.2:c.556A>G	XP_011528573.1:p.Met186Val
XM_011530272.2:c.661A>G	XP_011528574.1:p.Met221Val
XM_011530273.2:c.661A>G	XP_011528575.1:p.Met221Val
XM_011530274.2:c.319A>G	XP_011528576.1:p.Met107Val
XM_024452260.1:c.556A>G	XP_024308028.1:p.Met186Val
XR_001755261.2:n.707A>G
XR_001755262.2:n.707A>G
NM_018006.5:c.661A>G MANE Select	NP_060476.2:p.Met221Val
NM_001282782.2:c.319A>G	NP_001269711.1:p.Met107Val
NM_001282783.2:c.241A>G	NP_001269712.1:p.Met81Val
NM_001282784.2:c.241A>G	NP_001269713.1:p.Met81Val
NM_001282785.2:c.661A>G	NP_001269714.1:p.Met221Val
NR_104240.2:n.657A>G
NR_104241.2:n.550A>G