Canonical Allele Identifier: CA2657374815

Gene: TRMU

Linked Data

• gnomAD v4: 22-46352085-TCTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.46352088_46352090del , CM000684.2:g.46352088_46352090del	GRCh38
NC_000022.10:g.46747985_46747987del , CM000684.1:g.46747985_46747987del	GRCh37
NC_000022.9:g.45126649_45126651del	NCBI36
NG_012173.1:g.21688_21690del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465378.6:n.700-33_700-31del
ENST00000642923.1:c.547-33_547-31del	ENSP00000494255.1:n.547-33_547-31del
ENST00000643137.1:c.547-33_547-31del	ENSP00000495331.1:n.547-33_547-31del
ENST00000644006.1:c.*96-33_*96-31del	ENSP00000493778.1:n.*96-33_*96-31del
ENST00000645026.1:n.703-33_703-31del
ENST00000645190.1:c.652-33_652-31del MANE Select	ENSP00000496496.1:n.652-33_652-31del
ENST00000647301.1:c.*96-33_*96-31del	ENSP00000496641.1:n.*96-33_*96-31del
ENST00000290846.8:c.652-33_652-31del	ENSP00000290846.4:n.652-33_652-31del
ENST00000381019.3:c.652-33_652-31del	ENSP00000370407.3:n.652-33_652-31del
ENST00000381021.7:c.*245-33_*245-31del	ENSP00000370409.3:n.*245-33_*245-31del
ENST00000441818.5:c.*186-33_*186-31del	ENSP00000393014.1:n.*186-33_*186-31del
ENST00000453630.5:c.*190-33_*190-31del	ENSP00000398488.1:n.*190-33_*190-31del
ENST00000456595.5:c.*186-33_*186-31del	ENSP00000413880.1:n.*186-33_*186-31del
ENST00000457572.5:c.*96-33_*96-31del	ENSP00000407700.1:n.*96-33_*96-31del
ENST00000463785.1:n.120-33_120-31del
ENST00000479648.1:n.439_441del
ENST00000485175.5:n.612-33_612-31del
ENST00000486620.5:n.694-33_694-31del
NM_001282782.1:c.310-33_310-31del	NP_001269711.1:n.310-33_310-31del
NM_001282783.1:c.232-33_232-31del	NP_001269712.1:n.232-33_232-31del
NM_001282784.1:c.232-33_232-31del	NP_001269713.1:n.232-33_232-31del
NM_001282785.1:c.652-33_652-31del	NP_001269714.1:n.652-33_652-31del
NM_018006.4:c.652-33_652-31del	NP_060476.2:n.652-33_652-31del
NR_104240.1:n.961-33_961-31del
NR_104241.1:n.854-33_854-31del
XM_005261678.1:c.256-33_256-31del	XP_005261735.1:n.256-33_256-31del
XM_005261681.1:c.256-33_256-31del	XP_005261738.1:n.256-33_256-31del
XM_011530271.1:c.547-33_547-31del	XP_011528573.1:n.547-33_547-31del
XM_011530272.1:c.652-33_652-31del	XP_011528574.1:n.652-33_652-31del
XM_011530273.1:c.652-33_652-31del	XP_011528575.1:n.652-33_652-31del
XM_011530274.1:c.310-33_310-31del	XP_011528576.1:n.310-33_310-31del
XM_011530275.1:c.256-33_256-31del	XP_011528577.1:n.256-33_256-31del
XM_011530271.2:c.547-33_547-31del	XP_011528573.1:n.547-33_547-31del
XM_011530272.2:c.652-33_652-31del	XP_011528574.1:n.652-33_652-31del
XM_011530273.2:c.652-33_652-31del	XP_011528575.1:n.652-33_652-31del
XM_011530274.2:c.310-33_310-31del	XP_011528576.1:n.310-33_310-31del
XM_024452260.1:c.547-33_547-31del	XP_024308028.1:n.547-33_547-31del
XR_001755261.2:n.698-33_698-31del
XR_001755262.2:n.698-33_698-31del
NM_018006.5:c.652-33_652-31del MANE Select	NP_060476.2:n.652-33_652-31del
NM_001282782.2:c.310-33_310-31del	NP_001269711.1:n.310-33_310-31del
NM_001282783.2:c.232-33_232-31del	NP_001269712.1:n.232-33_232-31del
NM_001282784.2:c.232-33_232-31del	NP_001269713.1:n.232-33_232-31del
NM_001282785.2:c.652-33_652-31del	NP_001269714.1:n.652-33_652-31del
NR_104240.2:n.648-33_648-31del
NR_104241.2:n.541-33_541-31del