Canonical Allele Identifier: CA2657374947

Gene: TRMU

Linked Data

• gnomAD v4: 22-46352336-GTGCAGACTC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.46352340_46352348del , CM000684.2:g.46352340_46352348del	GRCh38
NC_000022.10:g.46748237_46748245del , CM000684.1:g.46748237_46748245del	GRCh37
NC_000022.9:g.45126901_45126909del	NCBI36
NG_012173.1:g.21940_21948del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465378.6:n.830_838del
ENST00000642923.1:c.667+10_667+18del	ENSP00000494255.1:n.667+10_667+18del
ENST00000643137.1:c.667+10_667+18del	ENSP00000495331.1:n.667+10_667+18del
ENST00000644006.1:c.*216+10_*216+18del	ENSP00000493778.1:n.*216+10_*216+18del
ENST00000645026.1:n.823+10_823+18del
ENST00000645190.1:c.772+10_772+18del MANE Select	ENSP00000496496.1:n.772+10_772+18del
ENST00000647301.1:c.*216+10_*216+18del	ENSP00000496641.1:n.*216+10_*216+18del
ENST00000290846.8:c.772+10_772+18del	ENSP00000290846.4:n.772+10_772+18del
ENST00000381019.3:c.772+10_772+18del	ENSP00000370407.3:n.772+10_772+18del
ENST00000381021.7:c.*365+10_*365+18del	ENSP00000370409.3:n.*365+10_*365+18del
ENST00000441818.5:c.*306+10_*306+18del	ENSP00000393014.1:n.*306+10_*306+18del
ENST00000453630.5:c.*310+10_*310+18del	ENSP00000398488.1:n.*310+10_*310+18del
ENST00000456595.5:c.*306+10_*306+18del	ENSP00000413880.1:n.*306+10_*306+18del
ENST00000457572.5:c.*216+10_*216+18del	ENSP00000407700.1:n.*216+10_*216+18del
ENST00000463785.1:n.240+10_240+18del
NM_001282782.1:c.430+10_430+18del	NP_001269711.1:n.430+10_430+18del
NM_001282783.1:c.352+10_352+18del	NP_001269712.1:n.352+10_352+18del
NM_001282784.1:c.352+10_352+18del	NP_001269713.1:n.352+10_352+18del
NM_001282785.1:c.772+10_772+18del	NP_001269714.1:n.772+10_772+18del
NM_018006.4:c.772+10_772+18del	NP_060476.2:n.772+10_772+18del
NR_104240.1:n.1081+10_1081+18del
NR_104241.1:n.974+10_974+18del
XM_005261678.1:c.376+10_376+18del	XP_005261735.1:n.376+10_376+18del
XM_005261681.1:c.376+10_376+18del	XP_005261738.1:n.376+10_376+18del
XM_011530271.1:c.667+10_667+18del	XP_011528573.1:n.667+10_667+18del
XM_011530272.1:c.772+10_772+18del	XP_011528574.1:n.772+10_772+18del
XM_011530273.1:c.772+10_772+18del	XP_011528575.1:n.772+10_772+18del
XM_011530274.1:c.430+10_430+18del	XP_011528576.1:n.430+10_430+18del
XM_011530275.1:c.376+10_376+18del	XP_011528577.1:n.376+10_376+18del
XM_011530271.2:c.667+10_667+18del	XP_011528573.1:n.667+10_667+18del
XM_011530272.2:c.772+10_772+18del	XP_011528574.1:n.772+10_772+18del
XM_011530273.2:c.772+10_772+18del	XP_011528575.1:n.772+10_772+18del
XM_011530274.2:c.430+10_430+18del	XP_011528576.1:n.430+10_430+18del
XM_024452260.1:c.667+10_667+18del	XP_024308028.1:n.667+10_667+18del
XR_001755261.2:n.818+10_818+18del
XR_001755262.2:n.818+10_818+18del
NM_018006.5:c.772+10_772+18del MANE Select	NP_060476.2:n.772+10_772+18del
NM_001282782.2:c.430+10_430+18del	NP_001269711.1:n.430+10_430+18del
NM_001282783.2:c.352+10_352+18del	NP_001269712.1:n.352+10_352+18del
NM_001282784.2:c.352+10_352+18del	NP_001269713.1:n.352+10_352+18del
NM_001282785.2:c.772+10_772+18del	NP_001269714.1:n.772+10_772+18del
NR_104240.2:n.768+10_768+18del
NR_104241.2:n.661+10_661+18del