Canonical Allele Identifier: CA2408700871

Gene: TRMU

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465378.6:n.777C=
ENST00000642923.1:c.624C=	ENSP00000494255.1:p.His208=
ENST00000643137.1:c.624C=	ENSP00000495331.1:p.His208=
ENST00000644006.1:c.*173C=	ENSP00000493778.1:n.*173C=
ENST00000645026.1:n.780C=
ENST00000645190.1:c.729C= MANE Select	ENSP00000496496.1:p.His243=
ENST00000647301.1:c.*173C=	ENSP00000496641.1:n.*173C=
ENST00000290846.8:c.729C=	ENSP00000290846.4:p.His243=
ENST00000381019.3:c.729C=	ENSP00000370407.3:p.His243=
ENST00000381021.7:c.*322C=	ENSP00000370409.3:n.*322C=
ENST00000441818.5:c.*263C=	ENSP00000393014.1:n.*263C=
ENST00000453630.5:c.*267C=	ENSP00000398488.1:n.*267C=
ENST00000456595.5:c.*263C=	ENSP00000413880.1:n.*263C=
ENST00000457572.5:c.*173C=	ENSP00000407700.1:n.*173C=
ENST00000463785.1:n.197C=
ENST00000479648.1:n.549C=
ENST00000485175.5:n.689C=
ENST00000486620.5:n.771C=
NM_001282782.1:c.387C=	NP_001269711.1:p.His129=
NM_001282783.1:c.309C=	NP_001269712.1:p.His103=
NM_001282784.1:c.309C=	NP_001269713.1:p.His103=
NM_001282785.1:c.729C=	NP_001269714.1:p.His243=
NM_018006.4:c.729C=	NP_060476.2:p.His243=
NR_104240.1:n.1038C=
NR_104241.1:n.931C=
XM_005261678.1:c.333C=	XP_005261735.1:p.His111=
XM_005261681.1:c.333C=	XP_005261738.1:p.His111=
XM_011530271.1:c.624C=	XP_011528573.1:p.His208=
XM_011530272.1:c.729C=	XP_011528574.1:p.His243=
XM_011530273.1:c.729C=	XP_011528575.1:p.His243=
XM_011530274.1:c.387C=	XP_011528576.1:p.His129=
XM_011530275.1:c.333C=	XP_011528577.1:p.His111=
XM_011530271.2:c.624C=	XP_011528573.1:p.His208=
XM_011530272.2:c.729C=	XP_011528574.1:p.His243=
XM_011530273.2:c.729C=	XP_011528575.1:p.His243=
XM_011530274.2:c.387C=	XP_011528576.1:p.His129=
XM_024452260.1:c.624C=	XP_024308028.1:p.His208=
XR_001755261.2:n.775C=
XR_001755262.2:n.775C=
NM_018006.5:c.729C= MANE Select	NP_060476.2:p.His243=
NM_001282782.2:c.387C=	NP_001269711.1:p.His129=
NM_001282783.2:c.309C=	NP_001269712.1:p.His103=
NM_001282784.2:c.309C=	NP_001269713.1:p.His103=
NM_001282785.2:c.729C=	NP_001269714.1:p.His243=
NR_104240.2:n.725C=
NR_104241.2:n.618C=