Canonical Allele Identifier: CA325175832

Gene: TRMU

Linked Data

• dbSNP Id: rs1047315636
• MyVariant Identifiers: chr22:g.46748203_46748205del (hg19) ; chr22:g.46352306_46352308del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.46352308_46352310del , CM000684.2:g.46352308_46352310del	GRCh38
NC_000022.10:g.46748205_46748207del , CM000684.1:g.46748205_46748207del	GRCh37
NC_000022.9:g.45126869_45126871del	NCBI36
NG_012173.1:g.21908_21910del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465378.6:n.798_800del
ENST00000642923.1:c.645_647del	ENSP00000494255.1:p.Asn215del
ENST00000643137.1:c.645_647del	ENSP00000495331.1:p.Asn215del
ENST00000644006.1:c.*194_*196del	ENSP00000493778.1:n.*194_*196del
ENST00000645026.1:n.801_803del
ENST00000645190.1:c.750_752del MANE Select	ENSP00000496496.1:p.Asn250del
ENST00000647301.1:c.*194_*196del	ENSP00000496641.1:n.*194_*196del
ENST00000290846.8:c.750_752del	ENSP00000290846.4:p.Asn250del
ENST00000381019.3:c.750_752del	ENSP00000370407.3:p.Asn250del
ENST00000381021.7:c.*343_*345del	ENSP00000370409.3:n.*343_*345del
ENST00000441818.5:c.*284_*286del	ENSP00000393014.1:n.*284_*286del
ENST00000453630.5:c.*288_*290del	ENSP00000398488.1:n.*288_*290del
ENST00000456595.5:c.*284_*286del	ENSP00000413880.1:n.*284_*286del
ENST00000457572.5:c.*194_*196del	ENSP00000407700.1:n.*194_*196del
ENST00000463785.1:n.218_220del
ENST00000479648.1:n.570_572del
ENST00000485175.5:n.710_712del
ENST00000486620.5:n.792_794del
NM_001282782.1:c.408_410del	NP_001269711.1:p.Asn136del
NM_001282783.1:c.330_332del	NP_001269712.1:p.Asn110del
NM_001282784.1:c.330_332del	NP_001269713.1:p.Asn110del
NM_001282785.1:c.750_752del	NP_001269714.1:p.Asn250del
NM_018006.4:c.750_752del	NP_060476.2:p.Asn250del
NR_104240.1:n.1059_1061del
NR_104241.1:n.952_954del
XM_005261678.1:c.354_356del	XP_005261735.1:p.Asn118del
XM_005261681.1:c.354_356del	XP_005261738.1:p.Asn118del
XM_011530271.1:c.645_647del	XP_011528573.1:p.Asn215del
XM_011530272.1:c.750_752del	XP_011528574.1:p.Asn250del
XM_011530273.1:c.750_752del	XP_011528575.1:p.Asn250del
XM_011530274.1:c.408_410del	XP_011528576.1:p.Asn136del
XM_011530275.1:c.354_356del	XP_011528577.1:p.Asn118del
XM_011530271.2:c.645_647del	XP_011528573.1:p.Asn215del
XM_011530272.2:c.750_752del	XP_011528574.1:p.Asn250del
XM_011530273.2:c.750_752del	XP_011528575.1:p.Asn250del
XM_011530274.2:c.408_410del	XP_011528576.1:p.Asn136del
XM_024452260.1:c.645_647del	XP_024308028.1:p.Asn215del
XR_001755261.2:n.796_798del
XR_001755262.2:n.796_798del
NM_018006.5:c.750_752del MANE Select	NP_060476.2:p.Asn250del
NM_001282782.2:c.408_410del	NP_001269711.1:p.Asn136del
NM_001282783.2:c.330_332del	NP_001269712.1:p.Asn110del
NM_001282784.2:c.330_332del	NP_001269713.1:p.Asn110del
NM_001282785.2:c.750_752del	NP_001269714.1:p.Asn250del
NR_104240.2:n.746_748del
NR_104241.2:n.639_641del