Canonical Allele Identifier: CA2408700690

Gene: TRMU

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.46352004_46352020delinsCTGGAAGCAAAGTGTGG , CM000684.2:g.46352004_46352020delinsCTGGAAGCAAAGTGTGG	GRCh38
NC_000022.10:g.46747901_46747917delinsCTGGAAGCAAAGTGTGG , CM000684.1:g.46747901_46747917delinsCTGGAAGCAAAGTGTGG	GRCh37
NC_000022.9:g.45126565_45126581delinsCTGGAAGCAAAGTGTGG	NCBI36
NG_012173.1:g.21604_21620delinsCTGGAAGCAAAGTGTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465378.6:n.700-117_700-101delinsCTGGAAGCAAAGTGTGG
ENST00000642923.1:c.547-117_547-101delinsCTGGAAGCAAAGTGTGG	ENSP00000494255.1:n.547-117_547-101delinsCTGGAAGCAAAGTGTGG
ENST00000643137.1:c.547-117_547-101delinsCTGGAAGCAAAGTGTGG	ENSP00000495331.1:n.547-117_547-101delinsCTGGAAGCAAAGTGTGG
ENST00000644006.1:c.*96-117_*96-101delinsCTGGAAGCAAAGTGTGG	ENSP00000493778.1:n.*96-117_*96-101delinsCTGGAAGCAAAGTGTGG
ENST00000645026.1:n.703-117_703-101delinsCTGGAAGCAAAGTGTGG
ENST00000645190.1:c.652-117_652-101delinsCTGGAAGCAAAGTGTGG MANE Select	ENSP00000496496.1:n.652-117_652-101delinsCTGGAAGCAAAGTGTGG
ENST00000647301.1:c.*96-117_*96-101delinsCTGGAAGCAAAGTGTGG	ENSP00000496641.1:n.*96-117_*96-101delinsCTGGAAGCAAAGTGTGG
ENST00000290846.8:c.652-117_652-101delinsCTGGAAGCAAAGTGTGG	ENSP00000290846.4:n.652-117_652-101delinsCTGGAAGCAAAGTGTGG
ENST00000381019.3:c.652-117_652-101delinsCTGGAAGCAAAGTGTGG	ENSP00000370407.3:n.652-117_652-101delinsCTGGAAGCAAAGTGTGG
ENST00000381021.7:c.*245-117_*245-101delinsCTGGAAGCAAAGTGTGG	ENSP00000370409.3:n.*245-117_*245-101delinsCTGGAAGCAAAGTGTGG
ENST00000441818.5:c.*186-117_*186-101delinsCTGGAAGCAAAGTGTGG	ENSP00000393014.1:n.*186-117_*186-101delinsCTGGAAGCAAAGTGTGG
ENST00000453630.5:c.*190-117_*190-101delinsCTGGAAGCAAAGTGTGG	ENSP00000398488.1:n.*190-117_*190-101delinsCTGGAAGCAAAGTGTGG
ENST00000456595.5:c.*186-117_*186-101delinsCTGGAAGCAAAGTGTGG	ENSP00000413880.1:n.*186-117_*186-101delinsCTGGAAGCAAAGTGTGG
ENST00000457572.5:c.*96-117_*96-101delinsCTGGAAGCAAAGTGTGG	ENSP00000407700.1:n.*96-117_*96-101delinsCTGGAAGCAAAGTGTGG
ENST00000463785.1:n.120-117_120-101delinsCTGGAAGCAAAGTGTGG
ENST00000479648.1:n.355_371delinsCTGGAAGCAAAGTGTGG
ENST00000485175.5:n.612-117_612-101delinsCTGGAAGCAAAGTGTGG
ENST00000486620.5:n.694-117_694-101delinsCTGGAAGCAAAGTGTGG
NM_001282782.1:c.310-117_310-101delinsCTGGAAGCAAAGTGTGG	NP_001269711.1:n.310-117_310-101delinsCTGGAAGCAAAGTGTGG
NM_001282783.1:c.232-117_232-101delinsCTGGAAGCAAAGTGTGG	NP_001269712.1:n.232-117_232-101delinsCTGGAAGCAAAGTGTGG
NM_001282784.1:c.232-117_232-101delinsCTGGAAGCAAAGTGTGG	NP_001269713.1:n.232-117_232-101delinsCTGGAAGCAAAGTGTGG
NM_001282785.1:c.652-117_652-101delinsCTGGAAGCAAAGTGTGG	NP_001269714.1:n.652-117_652-101delinsCTGGAAGCAAAGTGTGG
NM_018006.4:c.652-117_652-101delinsCTGGAAGCAAAGTGTGG	NP_060476.2:n.652-117_652-101delinsCTGGAAGCAAAGTGTGG
NR_104240.1:n.961-117_961-101delinsCTGGAAGCAAAGTGTGG
NR_104241.1:n.854-117_854-101delinsCTGGAAGCAAAGTGTGG
XM_005261678.1:c.256-117_256-101delinsCTGGAAGCAAAGTGTGG	XP_005261735.1:n.256-117_256-101delinsCTGGAAGCAAAGTGTGG
XM_005261681.1:c.256-117_256-101delinsCTGGAAGCAAAGTGTGG	XP_005261738.1:n.256-117_256-101delinsCTGGAAGCAAAGTGTGG
XM_011530271.1:c.547-117_547-101delinsCTGGAAGCAAAGTGTGG	XP_011528573.1:n.547-117_547-101delinsCTGGAAGCAAAGTGTGG
XM_011530272.1:c.652-117_652-101delinsCTGGAAGCAAAGTGTGG	XP_011528574.1:n.652-117_652-101delinsCTGGAAGCAAAGTGTGG
XM_011530273.1:c.652-117_652-101delinsCTGGAAGCAAAGTGTGG	XP_011528575.1:n.652-117_652-101delinsCTGGAAGCAAAGTGTGG
XM_011530274.1:c.310-117_310-101delinsCTGGAAGCAAAGTGTGG	XP_011528576.1:n.310-117_310-101delinsCTGGAAGCAAAGTGTGG
XM_011530275.1:c.256-117_256-101delinsCTGGAAGCAAAGTGTGG	XP_011528577.1:n.256-117_256-101delinsCTGGAAGCAAAGTGTGG
XM_011530271.2:c.547-117_547-101delinsCTGGAAGCAAAGTGTGG	XP_011528573.1:n.547-117_547-101delinsCTGGAAGCAAAGTGTGG
XM_011530272.2:c.652-117_652-101delinsCTGGAAGCAAAGTGTGG	XP_011528574.1:n.652-117_652-101delinsCTGGAAGCAAAGTGTGG
XM_011530273.2:c.652-117_652-101delinsCTGGAAGCAAAGTGTGG	XP_011528575.1:n.652-117_652-101delinsCTGGAAGCAAAGTGTGG
XM_011530274.2:c.310-117_310-101delinsCTGGAAGCAAAGTGTGG	XP_011528576.1:n.310-117_310-101delinsCTGGAAGCAAAGTGTGG
XM_024452260.1:c.547-117_547-101delinsCTGGAAGCAAAGTGTGG	XP_024308028.1:n.547-117_547-101delinsCTGGAAGCAAAGTGTGG
XR_001755261.2:n.698-117_698-101delinsCTGGAAGCAAAGTGTGG
XR_001755262.2:n.698-117_698-101delinsCTGGAAGCAAAGTGTGG
NM_018006.5:c.652-117_652-101delinsCTGGAAGCAAAGTGTGG MANE Select	NP_060476.2:n.652-117_652-101delinsCTGGAAGCAAAGTGTGG
NM_001282782.2:c.310-117_310-101delinsCTGGAAGCAAAGTGTGG	NP_001269711.1:n.310-117_310-101delinsCTGGAAGCAAAGTGTGG
NM_001282783.2:c.232-117_232-101delinsCTGGAAGCAAAGTGTGG	NP_001269712.1:n.232-117_232-101delinsCTGGAAGCAAAGTGTGG
NM_001282784.2:c.232-117_232-101delinsCTGGAAGCAAAGTGTGG	NP_001269713.1:n.232-117_232-101delinsCTGGAAGCAAAGTGTGG
NM_001282785.2:c.652-117_652-101delinsCTGGAAGCAAAGTGTGG	NP_001269714.1:n.652-117_652-101delinsCTGGAAGCAAAGTGTGG
NR_104240.2:n.648-117_648-101delinsCTGGAAGCAAAGTGTGG
NR_104241.2:n.541-117_541-101delinsCTGGAAGCAAAGTGTGG