Canonical Allele Identifier: CA2657374723

Gene: TRMU

Linked Data

• gnomAD v4: 22-46351967-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.46351968del , CM000684.2:g.46351968del	GRCh38
NC_000022.10:g.46747865del , CM000684.1:g.46747865del	GRCh37
NC_000022.9:g.45126529del	NCBI36
NG_012173.1:g.21568del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465378.6:n.700-153del
ENST00000642923.1:c.547-153del	ENSP00000494255.1:n.547-153del
ENST00000643137.1:c.547-153del	ENSP00000495331.1:n.547-153del
ENST00000644006.1:c.*96-153del	ENSP00000493778.1:n.*96-153del
ENST00000645026.1:n.703-153del
ENST00000645190.1:c.652-153del MANE Select	ENSP00000496496.1:n.652-153del
ENST00000647301.1:c.*96-153del	ENSP00000496641.1:n.*96-153del
ENST00000290846.8:c.652-153del	ENSP00000290846.4:n.652-153del
ENST00000381019.3:c.652-153del	ENSP00000370407.3:n.652-153del
ENST00000381021.7:c.*245-153del	ENSP00000370409.3:n.*245-153del
ENST00000441818.5:c.*186-153del	ENSP00000393014.1:n.*186-153del
ENST00000453630.5:c.*190-153del	ENSP00000398488.1:n.*190-153del
ENST00000456595.5:c.*186-153del	ENSP00000413880.1:n.*186-153del
ENST00000457572.5:c.*96-153del	ENSP00000407700.1:n.*96-153del
ENST00000463785.1:n.120-153del
ENST00000479648.1:n.319del
ENST00000485175.5:n.612-153del
ENST00000486620.5:n.694-153del
NM_001282782.1:c.310-153del	NP_001269711.1:n.310-153del
NM_001282783.1:c.232-153del	NP_001269712.1:n.232-153del
NM_001282784.1:c.232-153del	NP_001269713.1:n.232-153del
NM_001282785.1:c.652-153del	NP_001269714.1:n.652-153del
NM_018006.4:c.652-153del	NP_060476.2:n.652-153del
NR_104240.1:n.961-153del
NR_104241.1:n.854-153del
XM_005261678.1:c.256-153del	XP_005261735.1:n.256-153del
XM_005261681.1:c.256-153del	XP_005261738.1:n.256-153del
XM_011530271.1:c.547-153del	XP_011528573.1:n.547-153del
XM_011530272.1:c.652-153del	XP_011528574.1:n.652-153del
XM_011530273.1:c.652-153del	XP_011528575.1:n.652-153del
XM_011530274.1:c.310-153del	XP_011528576.1:n.310-153del
XM_011530275.1:c.256-153del	XP_011528577.1:n.256-153del
XM_011530271.2:c.547-153del	XP_011528573.1:n.547-153del
XM_011530272.2:c.652-153del	XP_011528574.1:n.652-153del
XM_011530273.2:c.652-153del	XP_011528575.1:n.652-153del
XM_011530274.2:c.310-153del	XP_011528576.1:n.310-153del
XM_024452260.1:c.547-153del	XP_024308028.1:n.547-153del
XR_001755261.2:n.698-153del
XR_001755262.2:n.698-153del
NM_018006.5:c.652-153del MANE Select	NP_060476.2:n.652-153del
NM_001282782.2:c.310-153del	NP_001269711.1:n.310-153del
NM_001282783.2:c.232-153del	NP_001269712.1:n.232-153del
NM_001282784.2:c.232-153del	NP_001269713.1:n.232-153del
NM_001282785.2:c.652-153del	NP_001269714.1:n.652-153del
NR_104240.2:n.648-153del
NR_104241.2:n.541-153del