Canonical Allele Identifier: CA411946421

Gene: TRMU

Linked Data

• dbSNP Id: rs1601977939
• gnomAD v4: 22-46352291-A-C
• MyVariant Identifiers: chr22:g.46748188A>C (hg19) ; chr22:g.46352291A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.46352291A>C , CM000684.2:g.46352291A>C	GRCh38
NC_000022.10:g.46748188A>C , CM000684.1:g.46748188A>C	GRCh37
NC_000022.9:g.45126852A>C	NCBI36
NG_012173.1:g.21891A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465378.6:n.781A>C
ENST00000642923.1:c.628A>C	ENSP00000494255.1:p.Ile210Leu
ENST00000643137.1:c.628A>C	ENSP00000495331.1:p.Ile210Leu
ENST00000644006.1:c.*177A>C	ENSP00000493778.1:n.*177A>C
ENST00000645026.1:n.784A>C
ENST00000645190.1:c.733A>C MANE Select	ENSP00000496496.1:p.Ile245Leu
ENST00000647301.1:c.*177A>C	ENSP00000496641.1:n.*177A>C
ENST00000290846.8:c.733A>C	ENSP00000290846.4:p.Ile245Leu
ENST00000381019.3:c.733A>C	ENSP00000370407.3:p.Ile245Leu
ENST00000381021.7:c.*326A>C	ENSP00000370409.3:n.*326A>C
ENST00000441818.5:c.*267A>C	ENSP00000393014.1:n.*267A>C
ENST00000453630.5:c.*271A>C	ENSP00000398488.1:n.*271A>C
ENST00000456595.5:c.*267A>C	ENSP00000413880.1:n.*267A>C
ENST00000457572.5:c.*177A>C	ENSP00000407700.1:n.*177A>C
ENST00000463785.1:n.201A>C
ENST00000479648.1:n.553A>C
ENST00000485175.5:n.693A>C
ENST00000486620.5:n.775A>C
NM_001282782.1:c.391A>C	NP_001269711.1:p.Ile131Leu
NM_001282783.1:c.313A>C	NP_001269712.1:p.Ile105Leu
NM_001282784.1:c.313A>C	NP_001269713.1:p.Ile105Leu
NM_001282785.1:c.733A>C	NP_001269714.1:p.Ile245Leu
NM_018006.4:c.733A>C	NP_060476.2:p.Ile245Leu
NR_104240.1:n.1042A>C
NR_104241.1:n.935A>C
XM_005261678.1:c.337A>C	XP_005261735.1:p.Ile113Leu
XM_005261681.1:c.337A>C	XP_005261738.1:p.Ile113Leu
XM_011530271.1:c.628A>C	XP_011528573.1:p.Ile210Leu
XM_011530272.1:c.733A>C	XP_011528574.1:p.Ile245Leu
XM_011530273.1:c.733A>C	XP_011528575.1:p.Ile245Leu
XM_011530274.1:c.391A>C	XP_011528576.1:p.Ile131Leu
XM_011530275.1:c.337A>C	XP_011528577.1:p.Ile113Leu
XM_011530271.2:c.628A>C	XP_011528573.1:p.Ile210Leu
XM_011530272.2:c.733A>C	XP_011528574.1:p.Ile245Leu
XM_011530273.2:c.733A>C	XP_011528575.1:p.Ile245Leu
XM_011530274.2:c.391A>C	XP_011528576.1:p.Ile131Leu
XM_024452260.1:c.628A>C	XP_024308028.1:p.Ile210Leu
XR_001755261.2:n.779A>C
XR_001755262.2:n.779A>C
NM_018006.5:c.733A>C MANE Select	NP_060476.2:p.Ile245Leu
NM_001282782.2:c.391A>C	NP_001269711.1:p.Ile131Leu
NM_001282783.2:c.313A>C	NP_001269712.1:p.Ile105Leu
NM_001282784.2:c.313A>C	NP_001269713.1:p.Ile105Leu
NM_001282785.2:c.733A>C	NP_001269714.1:p.Ile245Leu
NR_104240.2:n.729A>C
NR_104241.2:n.622A>C