Canonical Allele Identifier: CA2657374861

Gene: TRMU

Linked Data

• gnomAD v4: 22-46352265-ATCTGCAGCC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.46352268_46352276del , CM000684.2:g.46352268_46352276del	GRCh38
NC_000022.10:g.46748165_46748173del , CM000684.1:g.46748165_46748173del	GRCh37
NC_000022.9:g.45126829_45126837del	NCBI36
NG_012173.1:g.21868_21876del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465378.6:n.758_766del
ENST00000642923.1:c.605_613del	ENSP00000494255.1:p.Leu202_Pro204del
ENST00000643137.1:c.605_613del	ENSP00000495331.1:p.Leu202_Pro204del
ENST00000644006.1:c.*154_*162del	ENSP00000493778.1:n.*154_*162del
ENST00000645026.1:n.761_769del
ENST00000645190.1:c.710_718del MANE Select	ENSP00000496496.1:p.Leu237_Pro239del
ENST00000647301.1:c.*154_*162del	ENSP00000496641.1:n.*154_*162del
ENST00000290846.8:c.710_718del	ENSP00000290846.4:p.Leu237_Pro239del
ENST00000381019.3:c.710_718del	ENSP00000370407.3:p.Leu237_Pro239del
ENST00000381021.7:c.*303_*311del	ENSP00000370409.3:n.*303_*311del
ENST00000441818.5:c.*244_*252del	ENSP00000393014.1:n.*244_*252del
ENST00000453630.5:c.*248_*256del	ENSP00000398488.1:n.*248_*256del
ENST00000456595.5:c.*244_*252del	ENSP00000413880.1:n.*244_*252del
ENST00000457572.5:c.*154_*162del	ENSP00000407700.1:n.*154_*162del
ENST00000463785.1:n.178_186del
ENST00000479648.1:n.530_538del
ENST00000485175.5:n.670_678del
ENST00000486620.5:n.752_760del
NM_001282782.1:c.368_376del	NP_001269711.1:p.Leu123_Pro125del
NM_001282783.1:c.290_298del	NP_001269712.1:p.Leu97_Pro99del
NM_001282784.1:c.290_298del	NP_001269713.1:p.Leu97_Pro99del
NM_001282785.1:c.710_718del	NP_001269714.1:p.Leu237_Pro239del
NM_018006.4:c.710_718del	NP_060476.2:p.Leu237_Pro239del
NR_104240.1:n.1019_1027del
NR_104241.1:n.912_920del
XM_005261678.1:c.314_322del	XP_005261735.1:p.Leu105_Pro107del
XM_005261681.1:c.314_322del	XP_005261738.1:p.Leu105_Pro107del
XM_011530271.1:c.605_613del	XP_011528573.1:p.Leu202_Pro204del
XM_011530272.1:c.710_718del	XP_011528574.1:p.Leu237_Pro239del
XM_011530273.1:c.710_718del	XP_011528575.1:p.Leu237_Pro239del
XM_011530274.1:c.368_376del	XP_011528576.1:p.Leu123_Pro125del
XM_011530275.1:c.314_322del	XP_011528577.1:p.Leu105_Pro107del
XM_011530271.2:c.605_613del	XP_011528573.1:p.Leu202_Pro204del
XM_011530272.2:c.710_718del	XP_011528574.1:p.Leu237_Pro239del
XM_011530273.2:c.710_718del	XP_011528575.1:p.Leu237_Pro239del
XM_011530274.2:c.368_376del	XP_011528576.1:p.Leu123_Pro125del
XM_024452260.1:c.605_613del	XP_024308028.1:p.Leu202_Pro204del
XR_001755261.2:n.756_764del
XR_001755262.2:n.756_764del
NM_018006.5:c.710_718del MANE Select	NP_060476.2:p.Leu237_Pro239del
NM_001282782.2:c.368_376del	NP_001269711.1:p.Leu123_Pro125del
NM_001282783.2:c.290_298del	NP_001269712.1:p.Leu97_Pro99del
NM_001282784.2:c.290_298del	NP_001269713.1:p.Leu97_Pro99del
NM_001282785.2:c.710_718del	NP_001269714.1:p.Leu237_Pro239del
NR_104240.2:n.706_714del
NR_104241.2:n.599_607del