Canonical Allele Identifier: CA411946367

Gene: TRMU

Linked Data

• dbSNP Id: rs142972675
• gnomAD v2: 22-46748176-C-T
• gnomAD v4: 22-46352279-C-T
• MyVariant Identifiers: chr22:g.46748176C>T (hg19) ; chr22:g.46352279C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.46352279C>T , CM000684.2:g.46352279C>T	GRCh38
NC_000022.10:g.46748176C>T , CM000684.1:g.46748176C>T	GRCh37
NC_000022.9:g.45126840C>T	NCBI36
NG_012173.1:g.21879C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465378.6:n.769C>T
ENST00000642923.1:c.616C>T	ENSP00000494255.1:p.Pro206Ser
ENST00000643137.1:c.616C>T	ENSP00000495331.1:p.Pro206Ser
ENST00000644006.1:c.*165C>T	ENSP00000493778.1:n.*165C>T
ENST00000645026.1:n.772C>T
ENST00000645190.1:c.721C>T MANE Select	ENSP00000496496.1:p.Pro241Ser
ENST00000647301.1:c.*165C>T	ENSP00000496641.1:n.*165C>T
ENST00000290846.8:c.721C>T	ENSP00000290846.4:p.Pro241Ser
ENST00000381019.3:c.721C>T	ENSP00000370407.3:p.Pro241Ser
ENST00000381021.7:c.*314C>T	ENSP00000370409.3:n.*314C>T
ENST00000441818.5:c.*255C>T	ENSP00000393014.1:n.*255C>T
ENST00000453630.5:c.*259C>T	ENSP00000398488.1:n.*259C>T
ENST00000456595.5:c.*255C>T	ENSP00000413880.1:n.*255C>T
ENST00000457572.5:c.*165C>T	ENSP00000407700.1:n.*165C>T
ENST00000463785.1:n.189C>T
ENST00000479648.1:n.541C>T
ENST00000485175.5:n.681C>T
ENST00000486620.5:n.763C>T
NM_001282782.1:c.379C>T	NP_001269711.1:p.Pro127Ser
NM_001282783.1:c.301C>T	NP_001269712.1:p.Pro101Ser
NM_001282784.1:c.301C>T	NP_001269713.1:p.Pro101Ser
NM_001282785.1:c.721C>T	NP_001269714.1:p.Pro241Ser
NM_018006.4:c.721C>T	NP_060476.2:p.Pro241Ser
NR_104240.1:n.1030C>T
NR_104241.1:n.923C>T
XM_005261678.1:c.325C>T	XP_005261735.1:p.Pro109Ser
XM_005261681.1:c.325C>T	XP_005261738.1:p.Pro109Ser
XM_011530271.1:c.616C>T	XP_011528573.1:p.Pro206Ser
XM_011530272.1:c.721C>T	XP_011528574.1:p.Pro241Ser
XM_011530273.1:c.721C>T	XP_011528575.1:p.Pro241Ser
XM_011530274.1:c.379C>T	XP_011528576.1:p.Pro127Ser
XM_011530275.1:c.325C>T	XP_011528577.1:p.Pro109Ser
XM_011530271.2:c.616C>T	XP_011528573.1:p.Pro206Ser
XM_011530272.2:c.721C>T	XP_011528574.1:p.Pro241Ser
XM_011530273.2:c.721C>T	XP_011528575.1:p.Pro241Ser
XM_011530274.2:c.379C>T	XP_011528576.1:p.Pro127Ser
XM_024452260.1:c.616C>T	XP_024308028.1:p.Pro206Ser
XR_001755261.2:n.767C>T
XR_001755262.2:n.767C>T
NM_018006.5:c.721C>T MANE Select	NP_060476.2:p.Pro241Ser
NM_001282782.2:c.379C>T	NP_001269711.1:p.Pro127Ser
NM_001282783.2:c.301C>T	NP_001269712.1:p.Pro101Ser
NM_001282784.2:c.301C>T	NP_001269713.1:p.Pro101Ser
NM_001282785.2:c.721C>T	NP_001269714.1:p.Pro241Ser
NR_104240.2:n.717C>T
NR_104241.2:n.610C>T