Canonical Allele Identifier: CA514925575

Gene: TRMU

Linked Data

• MyVariant Identifiers: chr22:g.46748178T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.46352281T>A , CM000684.2:g.46352281T>A	GRCh38
NC_000022.10:g.46748178T>A , CM000684.1:g.46748178T>A	GRCh37
NC_000022.9:g.45126842T>A	NCBI36
NG_012173.1:g.21881T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465378.6:n.771T>A
ENST00000642923.1:c.618T>A	ENSP00000494255.1:p.Pro206=
ENST00000643137.1:c.618T>A	ENSP00000495331.1:p.Pro206=
ENST00000644006.1:c.*167T>A	ENSP00000493778.1:n.*167T>A
ENST00000645026.1:n.774T>A
ENST00000645190.1:c.723T>A MANE Select	ENSP00000496496.1:p.Pro241=
ENST00000647301.1:c.*167T>A	ENSP00000496641.1:n.*167T>A
ENST00000290846.8:c.723T>A	ENSP00000290846.4:p.Pro241=
ENST00000381019.3:c.723T>A	ENSP00000370407.3:p.Pro241=
ENST00000381021.7:c.*316T>A	ENSP00000370409.3:n.*316T>A
ENST00000441818.5:c.*257T>A	ENSP00000393014.1:n.*257T>A
ENST00000453630.5:c.*261T>A	ENSP00000398488.1:n.*261T>A
ENST00000456595.5:c.*257T>A	ENSP00000413880.1:n.*257T>A
ENST00000457572.5:c.*167T>A	ENSP00000407700.1:n.*167T>A
ENST00000463785.1:n.191T>A
ENST00000479648.1:n.543T>A
ENST00000485175.5:n.683T>A
ENST00000486620.5:n.765T>A
NM_001282782.1:c.381T>A	NP_001269711.1:p.Pro127=
NM_001282783.1:c.303T>A	NP_001269712.1:p.Pro101=
NM_001282784.1:c.303T>A	NP_001269713.1:p.Pro101=
NM_001282785.1:c.723T>A	NP_001269714.1:p.Pro241=
NM_018006.4:c.723T>A	NP_060476.2:p.Pro241=
NR_104240.1:n.1032T>A
NR_104241.1:n.925T>A
XM_005261678.1:c.327T>A	XP_005261735.1:p.Pro109=
XM_005261681.1:c.327T>A	XP_005261738.1:p.Pro109=
XM_011530271.1:c.618T>A	XP_011528573.1:p.Pro206=
XM_011530272.1:c.723T>A	XP_011528574.1:p.Pro241=
XM_011530273.1:c.723T>A	XP_011528575.1:p.Pro241=
XM_011530274.1:c.381T>A	XP_011528576.1:p.Pro127=
XM_011530275.1:c.327T>A	XP_011528577.1:p.Pro109=
XM_011530271.2:c.618T>A	XP_011528573.1:p.Pro206=
XM_011530272.2:c.723T>A	XP_011528574.1:p.Pro241=
XM_011530273.2:c.723T>A	XP_011528575.1:p.Pro241=
XM_011530274.2:c.381T>A	XP_011528576.1:p.Pro127=
XM_024452260.1:c.618T>A	XP_024308028.1:p.Pro206=
XR_001755261.2:n.769T>A
XR_001755262.2:n.769T>A
NM_018006.5:c.723T>A MANE Select	NP_060476.2:p.Pro241=
NM_001282782.2:c.381T>A	NP_001269711.1:p.Pro127=
NM_001282783.2:c.303T>A	NP_001269712.1:p.Pro101=
NM_001282784.2:c.303T>A	NP_001269713.1:p.Pro101=
NM_001282785.2:c.723T>A	NP_001269714.1:p.Pro241=
NR_104240.2:n.719T>A
NR_104241.2:n.612T>A