Canonical Allele Identifier: CA411940506

Gene: TRMU

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.46337940T>C , CM000684.2:g.46337940T>C	GRCh38
NC_000022.10:g.46733837T>C , CM000684.1:g.46733837T>C	GRCh37
NC_000022.9:g.45112501T>C	NCBI36
NG_012173.1:g.7540T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465378.6:n.347T>C
ENST00000493556.2:n.320T>C
ENST00000642562.1:c.82+2094T>C	ENSP00000494679.1:n.82+2094T>C
ENST00000642923.1:c.139T>C	ENSP00000494255.1:p.Phe47Leu
ENST00000643137.1:c.139T>C	ENSP00000495331.1:p.Phe47Leu
ENST00000644006.1:c.139T>C	ENSP00000493778.1:p.Phe47Leu
ENST00000645026.1:n.295T>C
ENST00000645190.1:c.244T>C MANE Select	ENSP00000496496.1:p.Phe82Leu
ENST00000647301.1:c.244T>C	ENSP00000496641.1:p.Phe82Leu
ENST00000290846.8:c.244T>C	ENSP00000290846.4:p.Phe82Leu
ENST00000381019.3:c.244T>C	ENSP00000370407.3:p.Phe82Leu
ENST00000381021.7:c.244T>C	ENSP00000370409.3:p.Phe82Leu
ENST00000441818.5:c.244T>C	ENSP00000393014.1:p.Phe82Leu
ENST00000453630.5:c.244T>C	ENSP00000398488.1:p.Phe82Leu
ENST00000456595.5:c.244T>C	ENSP00000413880.1:p.Phe82Leu
ENST00000457572.5:c.244T>C	ENSP00000407700.1:p.Phe82Leu
ENST00000465378.5:n.376T>C
ENST00000485175.5:n.311T>C
ENST00000486620.5:n.448T>C
ENST00000496831.5:n.374T>C
NM_001282782.1:c.9T>C	NP_001269711.1:p.Cys3=
NM_001282783.1:c.-11T>C	NP_001269712.1:n.-11T>C
NM_001282784.1:c.-11T>C	NP_001269713.1:n.-11T>C
NM_001282785.1:c.244T>C	NP_001269714.1:p.Phe82Leu
NM_018006.4:c.244T>C	NP_060476.2:p.Phe82Leu
NR_104240.1:n.608T>C
NR_104241.1:n.608T>C
XM_005261678.1:c.-94T>C	XP_005261735.1:n.-94T>C
XM_005261681.1:c.-94T>C	XP_005261738.1:n.-94T>C
XM_011530271.1:c.139T>C	XP_011528573.1:p.Phe47Leu
XM_011530272.1:c.244T>C	XP_011528574.1:p.Phe82Leu
XM_011530273.1:c.244T>C	XP_011528575.1:p.Phe82Leu
XM_011530274.1:c.9T>C	XP_011528576.1:p.Cys3=
XM_011530275.1:c.-94T>C	XP_011528577.1:n.-94T>C
XM_011530271.2:c.139T>C	XP_011528573.1:p.Phe47Leu
XM_011530272.2:c.244T>C	XP_011528574.1:p.Phe82Leu
XM_011530273.2:c.244T>C	XP_011528575.1:p.Phe82Leu
XM_011530274.2:c.9T>C	XP_011528576.1:p.Cys3=
XM_024452260.1:c.139T>C	XP_024308028.1:p.Phe47Leu
XR_001755261.2:n.290T>C
XR_001755262.2:n.290T>C
NM_018006.5:c.244T>C MANE Select	NP_060476.2:p.Phe82Leu
NM_001282782.2:c.9T>C	NP_001269711.1:p.Cys3=
NM_001282783.2:c.-11T>C	NP_001269712.1:n.-11T>C
NM_001282784.2:c.-11T>C	NP_001269713.1:n.-11T>C
NM_001282785.2:c.244T>C	NP_001269714.1:p.Phe82Leu
NR_104240.2:n.295T>C
NR_104241.2:n.295T>C