Canonical Allele Identifier: CA411946402

Gene: TRMU

Linked Data

• MyVariant Identifiers: chr22:g.46748184C>A (hg19) ; chr22:g.46352287C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.46352287C>A , CM000684.2:g.46352287C>A	GRCh38
NC_000022.10:g.46748184C>A , CM000684.1:g.46748184C>A	GRCh37
NC_000022.9:g.45126848C>A	NCBI36
NG_012173.1:g.21887C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465378.6:n.777C>A
ENST00000642923.1:c.624C>A	ENSP00000494255.1:p.His208Gln
ENST00000643137.1:c.624C>A	ENSP00000495331.1:p.His208Gln
ENST00000644006.1:c.*173C>A	ENSP00000493778.1:n.*173C>A
ENST00000645026.1:n.780C>A
ENST00000645190.1:c.729C>A MANE Select	ENSP00000496496.1:p.His243Gln
ENST00000647301.1:c.*173C>A	ENSP00000496641.1:n.*173C>A
ENST00000290846.8:c.729C>A	ENSP00000290846.4:p.His243Gln
ENST00000381019.3:c.729C>A	ENSP00000370407.3:p.His243Gln
ENST00000381021.7:c.*322C>A	ENSP00000370409.3:n.*322C>A
ENST00000441818.5:c.*263C>A	ENSP00000393014.1:n.*263C>A
ENST00000453630.5:c.*267C>A	ENSP00000398488.1:n.*267C>A
ENST00000456595.5:c.*263C>A	ENSP00000413880.1:n.*263C>A
ENST00000457572.5:c.*173C>A	ENSP00000407700.1:n.*173C>A
ENST00000463785.1:n.197C>A
ENST00000479648.1:n.549C>A
ENST00000485175.5:n.689C>A
ENST00000486620.5:n.771C>A
NM_001282782.1:c.387C>A	NP_001269711.1:p.His129Gln
NM_001282783.1:c.309C>A	NP_001269712.1:p.His103Gln
NM_001282784.1:c.309C>A	NP_001269713.1:p.His103Gln
NM_001282785.1:c.729C>A	NP_001269714.1:p.His243Gln
NM_018006.4:c.729C>A	NP_060476.2:p.His243Gln
NR_104240.1:n.1038C>A
NR_104241.1:n.931C>A
XM_005261678.1:c.333C>A	XP_005261735.1:p.His111Gln
XM_005261681.1:c.333C>A	XP_005261738.1:p.His111Gln
XM_011530271.1:c.624C>A	XP_011528573.1:p.His208Gln
XM_011530272.1:c.729C>A	XP_011528574.1:p.His243Gln
XM_011530273.1:c.729C>A	XP_011528575.1:p.His243Gln
XM_011530274.1:c.387C>A	XP_011528576.1:p.His129Gln
XM_011530275.1:c.333C>A	XP_011528577.1:p.His111Gln
XM_011530271.2:c.624C>A	XP_011528573.1:p.His208Gln
XM_011530272.2:c.729C>A	XP_011528574.1:p.His243Gln
XM_011530273.2:c.729C>A	XP_011528575.1:p.His243Gln
XM_011530274.2:c.387C>A	XP_011528576.1:p.His129Gln
XM_024452260.1:c.624C>A	XP_024308028.1:p.His208Gln
XR_001755261.2:n.775C>A
XR_001755262.2:n.775C>A
NM_018006.5:c.729C>A MANE Select	NP_060476.2:p.His243Gln
NM_001282782.2:c.387C>A	NP_001269711.1:p.His129Gln
NM_001282783.2:c.309C>A	NP_001269712.1:p.His103Gln
NM_001282784.2:c.309C>A	NP_001269713.1:p.His103Gln
NM_001282785.2:c.729C>A	NP_001269714.1:p.His243Gln
NR_104240.2:n.725C>A
NR_104241.2:n.618C>A