Canonical Allele Identifier: CA411946121

Gene: TRMU

Linked Data

• MyVariant Identifiers: chr22:g.46748024G>T (hg19) ; chr22:g.46352127G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.46352127G>T , CM000684.2:g.46352127G>T	GRCh38
NC_000022.10:g.46748024G>T , CM000684.1:g.46748024G>T	GRCh37
NC_000022.9:g.45126688G>T	NCBI36
NG_012173.1:g.21727G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465378.6:n.706G>T
ENST00000642923.1:c.553G>T	ENSP00000494255.1:p.Gly185Cys
ENST00000643137.1:c.553G>T	ENSP00000495331.1:p.Gly185Cys
ENST00000644006.1:c.*102G>T	ENSP00000493778.1:n.*102G>T
ENST00000645026.1:n.709G>T
ENST00000645190.1:c.658G>T MANE Select	ENSP00000496496.1:p.Gly220Cys
ENST00000647301.1:c.*102G>T	ENSP00000496641.1:n.*102G>T
ENST00000290846.8:c.658G>T	ENSP00000290846.4:p.Gly220Cys
ENST00000381019.3:c.658G>T	ENSP00000370407.3:p.Gly220Cys
ENST00000381021.7:c.*251G>T	ENSP00000370409.3:n.*251G>T
ENST00000441818.5:c.*192G>T	ENSP00000393014.1:n.*192G>T
ENST00000453630.5:c.*196G>T	ENSP00000398488.1:n.*196G>T
ENST00000456595.5:c.*192G>T	ENSP00000413880.1:n.*192G>T
ENST00000457572.5:c.*102G>T	ENSP00000407700.1:n.*102G>T
ENST00000463785.1:n.126G>T
ENST00000479648.1:n.478G>T
ENST00000485175.5:n.618G>T
ENST00000486620.5:n.700G>T
NM_001282782.1:c.316G>T	NP_001269711.1:p.Gly106Cys
NM_001282783.1:c.238G>T	NP_001269712.1:p.Gly80Cys
NM_001282784.1:c.238G>T	NP_001269713.1:p.Gly80Cys
NM_001282785.1:c.658G>T	NP_001269714.1:p.Gly220Cys
NM_018006.4:c.658G>T	NP_060476.2:p.Gly220Cys
NR_104240.1:n.967G>T
NR_104241.1:n.860G>T
XM_005261678.1:c.262G>T	XP_005261735.1:p.Gly88Cys
XM_005261681.1:c.262G>T	XP_005261738.1:p.Gly88Cys
XM_011530271.1:c.553G>T	XP_011528573.1:p.Gly185Cys
XM_011530272.1:c.658G>T	XP_011528574.1:p.Gly220Cys
XM_011530273.1:c.658G>T	XP_011528575.1:p.Gly220Cys
XM_011530274.1:c.316G>T	XP_011528576.1:p.Gly106Cys
XM_011530275.1:c.262G>T	XP_011528577.1:p.Gly88Cys
XM_011530271.2:c.553G>T	XP_011528573.1:p.Gly185Cys
XM_011530272.2:c.658G>T	XP_011528574.1:p.Gly220Cys
XM_011530273.2:c.658G>T	XP_011528575.1:p.Gly220Cys
XM_011530274.2:c.316G>T	XP_011528576.1:p.Gly106Cys
XM_024452260.1:c.553G>T	XP_024308028.1:p.Gly185Cys
XR_001755261.2:n.704G>T
XR_001755262.2:n.704G>T
NM_018006.5:c.658G>T MANE Select	NP_060476.2:p.Gly220Cys
NM_001282782.2:c.316G>T	NP_001269711.1:p.Gly106Cys
NM_001282783.2:c.238G>T	NP_001269712.1:p.Gly80Cys
NM_001282784.2:c.238G>T	NP_001269713.1:p.Gly80Cys
NM_001282785.2:c.658G>T	NP_001269714.1:p.Gly220Cys
NR_104240.2:n.654G>T
NR_104241.2:n.547G>T