Canonical Allele Identifier: CA753656457

Gene: TRMU

Linked Data

• dbSNP Id: rs1426761006
• MyVariant Identifiers: chr22:g.46748425_46748454del (hg19) ; chr22:g.46352528_46352557del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.46352528_46352557del , CM000684.2:g.46352528_46352557del	GRCh38
NC_000022.10:g.46748425_46748454del , CM000684.1:g.46748425_46748454del	GRCh37
NC_000022.9:g.45127089_45127118del	NCBI36
NG_012173.1:g.22128_22157del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465378.6:n.1018_1047del
ENST00000642923.1:c.667+198_667+227del	ENSP00000494255.1:n.667+198_667+227del
ENST00000643137.1:c.667+198_667+227del	ENSP00000495331.1:n.667+198_667+227del
ENST00000644006.1:c.*216+198_*216+227del	ENSP00000493778.1:n.*216+198_*216+227del
ENST00000645026.1:n.823+198_823+227del
ENST00000645190.1:c.772+198_772+227del MANE Select	ENSP00000496496.1:n.772+198_772+227del
ENST00000647301.1:c.*216+198_*216+227del	ENSP00000496641.1:n.*216+198_*216+227del
ENST00000290846.8:c.772+198_772+227del	ENSP00000290846.4:n.772+198_772+227del
ENST00000381019.3:c.772+198_772+227del	ENSP00000370407.3:n.772+198_772+227del
ENST00000381021.7:c.*365+198_*365+227del	ENSP00000370409.3:n.*365+198_*365+227del
ENST00000441818.5:c.*306+198_*306+227del	ENSP00000393014.1:n.*306+198_*306+227del
ENST00000453630.5:c.*310+198_*310+227del	ENSP00000398488.1:n.*310+198_*310+227del
ENST00000456595.5:c.*306+198_*306+227del	ENSP00000413880.1:n.*306+198_*306+227del
ENST00000457572.5:c.*216+198_*216+227del	ENSP00000407700.1:n.*216+198_*216+227del
ENST00000463785.1:n.244_273del
NM_001282782.1:c.430+198_430+227del	NP_001269711.1:n.430+198_430+227del
NM_001282783.1:c.352+198_352+227del	NP_001269712.1:n.352+198_352+227del
NM_001282784.1:c.352+198_352+227del	NP_001269713.1:n.352+198_352+227del
NM_001282785.1:c.772+198_772+227del	NP_001269714.1:n.772+198_772+227del
NM_018006.4:c.772+198_772+227del	NP_060476.2:n.772+198_772+227del
NR_104240.1:n.1081+198_1081+227del
NR_104241.1:n.974+198_974+227del
XM_005261678.1:c.376+198_376+227del	XP_005261735.1:n.376+198_376+227del
XM_005261681.1:c.376+198_376+227del	XP_005261738.1:n.376+198_376+227del
XM_011530271.1:c.667+198_667+227del	XP_011528573.1:n.667+198_667+227del
XM_011530272.1:c.772+198_772+227del	XP_011528574.1:n.772+198_772+227del
XM_011530273.1:c.772+198_772+227del	XP_011528575.1:n.772+198_772+227del
XM_011530274.1:c.430+198_430+227del	XP_011528576.1:n.430+198_430+227del
XM_011530275.1:c.376+198_376+227del	XP_011528577.1:n.376+198_376+227del
XM_011530271.2:c.667+198_667+227del	XP_011528573.1:n.667+198_667+227del
XM_011530272.2:c.772+198_772+227del	XP_011528574.1:n.772+198_772+227del
XM_011530273.2:c.772+198_772+227del	XP_011528575.1:n.772+198_772+227del
XM_011530274.2:c.430+198_430+227del	XP_011528576.1:n.430+198_430+227del
XM_024452260.1:c.667+198_667+227del	XP_024308028.1:n.667+198_667+227del
XR_001755261.2:n.822_851del
XR_001755262.2:n.822_851del
NM_018006.5:c.772+198_772+227del MANE Select	NP_060476.2:n.772+198_772+227del
NM_001282782.2:c.430+198_430+227del	NP_001269711.1:n.430+198_430+227del
NM_001282783.2:c.352+198_352+227del	NP_001269712.1:n.352+198_352+227del
NM_001282784.2:c.352+198_352+227del	NP_001269713.1:n.352+198_352+227del
NM_001282785.2:c.772+198_772+227del	NP_001269714.1:n.772+198_772+227del
NR_104240.2:n.768+198_768+227del
NR_104241.2:n.661+198_661+227del