Canonical Allele Identifier: CA324933

Gene: TRMU

Linked Data

• ClinVar Variation Id: 215287
• ClinVar RCV Id: RCV000200369 ; RCV001273736 ; RCV003474950
• dbSNP Id: rs367683258
• ExAC: 22:46748173 C / T
• gnomAD v2: 22-46748173-C-T
• gnomAD v3: 22-46352276-C-T
• gnomAD v4: 22-46352276-C-T
• MyVariant Identifiers: chr22:g.46748173C>T (hg19) ; chr22:g.46352276C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.46352276C>T , CM000684.2:g.46352276C>T	GRCh38
NC_000022.10:g.46748173C>T , CM000684.1:g.46748173C>T	GRCh37
NC_000022.9:g.45126837C>T	NCBI36
NG_012173.1:g.21876C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465378.6:n.766C>T
ENST00000642923.1:c.613C>T	ENSP00000494255.1:p.Arg205Ter
ENST00000643137.1:c.613C>T	ENSP00000495331.1:p.Arg205Ter
ENST00000644006.1:c.*162C>T	ENSP00000493778.1:n.*162C>T
ENST00000645026.1:n.769C>T
ENST00000645190.1:c.718C>T MANE Select	ENSP00000496496.1:p.Arg240Ter
ENST00000647301.1:c.*162C>T	ENSP00000496641.1:n.*162C>T
ENST00000290846.8:c.718C>T	ENSP00000290846.4:p.Arg240Ter
ENST00000381019.3:c.718C>T	ENSP00000370407.3:p.Arg240Ter
ENST00000381021.7:c.*311C>T	ENSP00000370409.3:n.*311C>T
ENST00000441818.5:c.*252C>T	ENSP00000393014.1:n.*252C>T
ENST00000453630.5:c.*256C>T	ENSP00000398488.1:n.*256C>T
ENST00000456595.5:c.*252C>T	ENSP00000413880.1:n.*252C>T
ENST00000457572.5:c.*162C>T	ENSP00000407700.1:n.*162C>T
ENST00000463785.1:n.186C>T
ENST00000479648.1:n.538C>T
ENST00000485175.5:n.678C>T
ENST00000486620.5:n.760C>T
NM_001282782.1:c.376C>T	NP_001269711.1:p.Arg126Ter
NM_001282783.1:c.298C>T	NP_001269712.1:p.Arg100Ter
NM_001282784.1:c.298C>T	NP_001269713.1:p.Arg100Ter
NM_001282785.1:c.718C>T	NP_001269714.1:p.Arg240Ter
NM_018006.4:c.718C>T	NP_060476.2:p.Arg240Ter
NR_104240.1:n.1027C>T
NR_104241.1:n.920C>T
XM_005261678.1:c.322C>T	XP_005261735.1:p.Arg108Ter
XM_005261681.1:c.322C>T	XP_005261738.1:p.Arg108Ter
XM_011530271.1:c.613C>T	XP_011528573.1:p.Arg205Ter
XM_011530272.1:c.718C>T	XP_011528574.1:p.Arg240Ter
XM_011530273.1:c.718C>T	XP_011528575.1:p.Arg240Ter
XM_011530274.1:c.376C>T	XP_011528576.1:p.Arg126Ter
XM_011530275.1:c.322C>T	XP_011528577.1:p.Arg108Ter
XM_011530271.2:c.613C>T	XP_011528573.1:p.Arg205Ter
XM_011530272.2:c.718C>T	XP_011528574.1:p.Arg240Ter
XM_011530273.2:c.718C>T	XP_011528575.1:p.Arg240Ter
XM_011530274.2:c.376C>T	XP_011528576.1:p.Arg126Ter
XM_024452260.1:c.613C>T	XP_024308028.1:p.Arg205Ter
XR_001755261.2:n.764C>T
XR_001755262.2:n.764C>T
NM_018006.5:c.718C>T MANE Select	NP_060476.2:p.Arg240Ter
NM_001282782.2:c.376C>T	NP_001269711.1:p.Arg126Ter
NM_001282783.2:c.298C>T	NP_001269712.1:p.Arg100Ter
NM_001282784.2:c.298C>T	NP_001269713.1:p.Arg100Ter
NM_001282785.2:c.718C>T	NP_001269714.1:p.Arg240Ter
NR_104240.2:n.714C>T
NR_104241.2:n.607C>T