Canonical Allele Identifier: CA411940492

Gene: TRMU

Linked Data

• MyVariant Identifiers: chr22:g.46733830T>G (hg19) ; chr22:g.46337933T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.46337933T>G , CM000684.2:g.46337933T>G	GRCh38
NC_000022.10:g.46733830T>G , CM000684.1:g.46733830T>G	GRCh37
NC_000022.9:g.45112494T>G	NCBI36
NG_012173.1:g.7533T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000465378.6:n.340T>G
ENST00000493556.2:n.313T>G
ENST00000642562.1:c.82+2087T>G	ENSP00000494679.1:n.82+2087T>G
ENST00000642923.1:c.132T>G	ENSP00000494255.1:p.Asn44Lys
ENST00000643137.1:c.132T>G	ENSP00000495331.1:p.Asn44Lys
ENST00000644006.1:c.132T>G	ENSP00000493778.1:p.Asn44Lys
ENST00000645026.1:n.288T>G
ENST00000645190.1:c.237T>G MANE Select	ENSP00000496496.1:p.Asn79Lys
ENST00000647301.1:c.237T>G	ENSP00000496641.1:p.Asn79Lys
ENST00000290846.8:c.237T>G	ENSP00000290846.4:p.Asn79Lys
ENST00000381019.3:c.237T>G	ENSP00000370407.3:p.Asn79Lys
ENST00000381021.7:c.237T>G	ENSP00000370409.3:p.Asn79Lys
ENST00000441818.5:c.237T>G	ENSP00000393014.1:p.Asn79Lys
ENST00000453630.5:c.237T>G	ENSP00000398488.1:p.Asn79Lys
ENST00000456595.5:c.237T>G	ENSP00000413880.1:p.Asn79Lys
ENST00000457572.5:c.237T>G	ENSP00000407700.1:p.Asn79Lys
ENST00000465378.5:n.369T>G
ENST00000485175.5:n.304T>G
ENST00000486620.5:n.441T>G
ENST00000493556.1:n.432T>G
ENST00000496831.5:n.367T>G
NM_001282782.1:c.2T>G	NP_001269711.1:p.Met1Arg
NM_001282783.1:c.-18T>G	NP_001269712.1:n.-18T>G
NM_001282784.1:c.-18T>G	NP_001269713.1:n.-18T>G
NM_001282785.1:c.237T>G	NP_001269714.1:p.Asn79Lys
NM_018006.4:c.237T>G	NP_060476.2:p.Asn79Lys
NR_104240.1:n.601T>G
NR_104241.1:n.601T>G
XM_005261678.1:c.-101T>G	XP_005261735.1:n.-101T>G
XM_005261681.1:c.-101T>G	XP_005261738.1:n.-101T>G
XM_011530271.1:c.132T>G	XP_011528573.1:p.Asn44Lys
XM_011530272.1:c.237T>G	XP_011528574.1:p.Asn79Lys
XM_011530273.1:c.237T>G	XP_011528575.1:p.Asn79Lys
XM_011530274.1:c.2T>G	XP_011528576.1:p.Met1Arg
XM_011530275.1:c.-101T>G	XP_011528577.1:n.-101T>G
XM_011530271.2:c.132T>G	XP_011528573.1:p.Asn44Lys
XM_011530272.2:c.237T>G	XP_011528574.1:p.Asn79Lys
XM_011530273.2:c.237T>G	XP_011528575.1:p.Asn79Lys
XM_011530274.2:c.2T>G	XP_011528576.1:p.Met1Arg
XM_024452260.1:c.132T>G	XP_024308028.1:p.Asn44Lys
XR_001755261.2:n.283T>G
XR_001755262.2:n.283T>G
NM_018006.5:c.237T>G MANE Select	NP_060476.2:p.Asn79Lys
NM_001282782.2:c.2T>G	NP_001269711.1:p.Met1Arg
NM_001282783.2:c.-18T>G	NP_001269712.1:n.-18T>G
NM_001282784.2:c.-18T>G	NP_001269713.1:n.-18T>G
NM_001282785.2:c.237T>G	NP_001269714.1:p.Asn79Lys
NR_104240.2:n.288T>G
NR_104241.2:n.288T>G