Canonical Allele Identifier: CA170799

Gene: TRMT10A

Linked Data

• ClinVar Variation Id: 156230
• ClinVar RCV Id: RCV000144248 ; RCV000624590
• dbSNP Id: rs587777744
• MyVariant Identifiers: chr4:g.100474971C>T (hg19) ; chr4:g.99553814C>T (hg38)
• PubMed: PMID:24204302 ; PMID:25053765 ; PMID:26297882 ; PMID:26526202 ; PMID:26535115

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99553814C>T , CM000666.2:g.99553814C>T	GRCh38
NC_000004.11:g.100474971C>T , CM000666.1:g.100474971C>T	GRCh37
NC_000004.10:g.100693994C>T	NCBI36
NG_041774.1:g.15244G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394876.7:c.616G>A MANE Select	ENSP00000378342.2:p.Gly206Arg
ENST00000273962.7:c.616G>A	ENSP00000273962.3:p.Gly206Arg
ENST00000394876.6:c.616G>A	ENSP00000378342.2:p.Gly206Arg
ENST00000394877.7:c.616G>A	ENSP00000378343.3:p.Gly206Arg
ENST00000455368.6:c.616G>A
NM_001134665.2:c.616G>A	NP_001128137.1:p.Gly206Arg
NM_001134666.2:c.616G>A	NP_001128138.1:p.Gly206Arg
NM_152292.4:c.616G>A	NP_689505.1:p.Gly206Arg
XM_005263352.3:c.616G>A	XP_005263409.1:p.Gly206Arg
XM_006714417.2:c.616G>A	XP_006714480.1:p.Gly206Arg
XM_006714418.2:c.616G>A	XP_006714481.1:p.Gly206Arg
NM_001134665.3:c.616G>A MANE Select	NP_001128137.1:p.Gly206Arg
NM_001134666.3:c.616G>A	NP_001128138.1:p.Gly206Arg
NM_001375880.1:c.616G>A	NP_001362809.1:p.Gly206Arg
NM_001375881.1:c.616G>A	NP_001362810.1:p.Gly206Arg
NM_001375882.1:c.616G>A	NP_001362811.1:p.Gly206Arg
NM_152292.5:c.616G>A	NP_689505.1:p.Gly206Arg