Canonical Allele Identifier: CA753656521

Gene: TRMU

Linked Data

• dbSNP Id: rs1437768085
• gnomAD v3: 22-46352590-CTG-C
• gnomAD v4: 22-46352590-CTG-C
• MyVariant Identifiers: chr22:g.46748488_46748489del (hg19) ; chr22:g.46352591_46352592del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.46352593_46352594del , CM000684.2:g.46352593_46352594del	GRCh38
NC_000022.10:g.46748490_46748491del , CM000684.1:g.46748490_46748491del	GRCh37
NC_000022.9:g.45127154_45127155del	NCBI36
NG_012173.1:g.22193_22194del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465378.6:n.1083_1084del
ENST00000642923.1:c.667+263_667+264del	ENSP00000494255.1:n.667+263_667+264del
ENST00000643137.1:c.667+263_667+264del	ENSP00000495331.1:n.667+263_667+264del
ENST00000644006.1:c.*216+263_*216+264del	ENSP00000493778.1:n.*216+263_*216+264del
ENST00000645026.1:n.823+263_823+264del
ENST00000645190.1:c.772+263_772+264del MANE Select	ENSP00000496496.1:n.772+263_772+264del
ENST00000647301.1:c.*216+263_*216+264del	ENSP00000496641.1:n.*216+263_*216+264del
ENST00000290846.8:c.772+263_772+264del	ENSP00000290846.4:n.772+263_772+264del
ENST00000381019.3:c.772+263_772+264del	ENSP00000370407.3:n.772+263_772+264del
ENST00000381021.7:c.*365+263_*365+264del	ENSP00000370409.3:n.*365+263_*365+264del
ENST00000441818.5:c.*306+263_*306+264del	ENSP00000393014.1:n.*306+263_*306+264del
ENST00000453630.5:c.*310+263_*310+264del	ENSP00000398488.1:n.*310+263_*310+264del
ENST00000456595.5:c.*306+263_*306+264del	ENSP00000413880.1:n.*306+263_*306+264del
ENST00000457572.5:c.*216+263_*216+264del	ENSP00000407700.1:n.*216+263_*216+264del
ENST00000463785.1:n.309_310del
NM_001282782.1:c.430+263_430+264del	NP_001269711.1:n.430+263_430+264del
NM_001282783.1:c.352+263_352+264del	NP_001269712.1:n.352+263_352+264del
NM_001282784.1:c.352+263_352+264del	NP_001269713.1:n.352+263_352+264del
NM_001282785.1:c.772+263_772+264del	NP_001269714.1:n.772+263_772+264del
NM_018006.4:c.772+263_772+264del	NP_060476.2:n.772+263_772+264del
NR_104240.1:n.1081+263_1081+264del
NR_104241.1:n.974+263_974+264del
XM_005261678.1:c.376+263_376+264del	XP_005261735.1:n.376+263_376+264del
XM_005261681.1:c.376+263_376+264del	XP_005261738.1:n.376+263_376+264del
XM_011530271.1:c.667+263_667+264del	XP_011528573.1:n.667+263_667+264del
XM_011530272.1:c.772+263_772+264del	XP_011528574.1:n.772+263_772+264del
XM_011530273.1:c.772+263_772+264del	XP_011528575.1:n.772+263_772+264del
XM_011530274.1:c.430+263_430+264del	XP_011528576.1:n.430+263_430+264del
XM_011530275.1:c.376+263_376+264del	XP_011528577.1:n.376+263_376+264del
XM_011530271.2:c.667+263_667+264del	XP_011528573.1:n.667+263_667+264del
XM_011530272.2:c.772+263_772+264del	XP_011528574.1:n.772+263_772+264del
XM_011530273.2:c.772+263_772+264del	XP_011528575.1:n.772+263_772+264del
XM_011530274.2:c.430+263_430+264del	XP_011528576.1:n.430+263_430+264del
XM_024452260.1:c.667+263_667+264del	XP_024308028.1:n.667+263_667+264del
XR_001755261.2:n.887_888del
XR_001755262.2:n.887_888del
NM_018006.5:c.772+263_772+264del MANE Select	NP_060476.2:n.772+263_772+264del
NM_001282782.2:c.430+263_430+264del	NP_001269711.1:n.430+263_430+264del
NM_001282783.2:c.352+263_352+264del	NP_001269712.1:n.352+263_352+264del
NM_001282784.2:c.352+263_352+264del	NP_001269713.1:n.352+263_352+264del
NM_001282785.2:c.772+263_772+264del	NP_001269714.1:n.772+263_772+264del
NR_104240.2:n.768+263_768+264del
NR_104241.2:n.661+263_661+264del