Canonical Allele Identifier: CA411946182

Gene: TRMU

Linked Data

• MyVariant Identifiers: chr22:g.46748052T>C (hg19) ; chr22:g.46352155T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.46352155T>C , CM000684.2:g.46352155T>C	GRCh38
NC_000022.10:g.46748052T>C , CM000684.1:g.46748052T>C	GRCh37
NC_000022.9:g.45126716T>C	NCBI36
NG_012173.1:g.21755T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465378.6:n.734T>C
ENST00000642923.1:c.581T>C	ENSP00000494255.1:p.Phe194Ser
ENST00000643137.1:c.581T>C	ENSP00000495331.1:p.Phe194Ser
ENST00000644006.1:c.*130T>C	ENSP00000493778.1:n.*130T>C
ENST00000645026.1:n.737T>C
ENST00000645190.1:c.686T>C MANE Select	ENSP00000496496.1:p.Phe229Ser
ENST00000647301.1:c.*130T>C	ENSP00000496641.1:n.*130T>C
ENST00000290846.8:c.686T>C	ENSP00000290846.4:p.Phe229Ser
ENST00000381019.3:c.686T>C	ENSP00000370407.3:p.Phe229Ser
ENST00000381021.7:c.*279T>C	ENSP00000370409.3:n.*279T>C
ENST00000441818.5:c.*220T>C	ENSP00000393014.1:n.*220T>C
ENST00000453630.5:c.*224T>C	ENSP00000398488.1:n.*224T>C
ENST00000456595.5:c.*220T>C	ENSP00000413880.1:n.*220T>C
ENST00000457572.5:c.*130T>C	ENSP00000407700.1:n.*130T>C
ENST00000463785.1:n.154T>C
ENST00000479648.1:n.506T>C
ENST00000485175.5:n.646T>C
ENST00000486620.5:n.728T>C
NM_001282782.1:c.344T>C	NP_001269711.1:p.Phe115Ser
NM_001282783.1:c.266T>C	NP_001269712.1:p.Phe89Ser
NM_001282784.1:c.266T>C	NP_001269713.1:p.Phe89Ser
NM_001282785.1:c.686T>C	NP_001269714.1:p.Phe229Ser
NM_018006.4:c.686T>C	NP_060476.2:p.Phe229Ser
NR_104240.1:n.995T>C
NR_104241.1:n.888T>C
XM_005261678.1:c.290T>C	XP_005261735.1:p.Phe97Ser
XM_005261681.1:c.290T>C	XP_005261738.1:p.Phe97Ser
XM_011530271.1:c.581T>C	XP_011528573.1:p.Phe194Ser
XM_011530272.1:c.686T>C	XP_011528574.1:p.Phe229Ser
XM_011530273.1:c.686T>C	XP_011528575.1:p.Phe229Ser
XM_011530274.1:c.344T>C	XP_011528576.1:p.Phe115Ser
XM_011530275.1:c.290T>C	XP_011528577.1:p.Phe97Ser
XM_011530271.2:c.581T>C	XP_011528573.1:p.Phe194Ser
XM_011530272.2:c.686T>C	XP_011528574.1:p.Phe229Ser
XM_011530273.2:c.686T>C	XP_011528575.1:p.Phe229Ser
XM_011530274.2:c.344T>C	XP_011528576.1:p.Phe115Ser
XM_024452260.1:c.581T>C	XP_024308028.1:p.Phe194Ser
XR_001755261.2:n.732T>C
XR_001755262.2:n.732T>C
NM_018006.5:c.686T>C MANE Select	NP_060476.2:p.Phe229Ser
NM_001282782.2:c.344T>C	NP_001269711.1:p.Phe115Ser
NM_001282783.2:c.266T>C	NP_001269712.1:p.Phe89Ser
NM_001282784.2:c.266T>C	NP_001269713.1:p.Phe89Ser
NM_001282785.2:c.686T>C	NP_001269714.1:p.Phe229Ser
NR_104240.2:n.682T>C
NR_104241.2:n.575T>C