Canonical Allele Identifier: CA357510930

Gene: TRMT10A

Linked Data

• MyVariant Identifiers: chr4:g.100478556A>C (hg19) ; chr4:g.99557399A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99557399A>C , CM000666.2:g.99557399A>C	GRCh38
NC_000004.11:g.100478556A>C , CM000666.1:g.100478556A>C	GRCh37
NC_000004.10:g.100697579A>C	NCBI36
NG_041774.1:g.11659T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000394876.7:c.366T>G MANE Select	ENSP00000378342.2:p.His122Gln
ENST00000273962.7:c.366T>G	ENSP00000273962.3:p.His122Gln
ENST00000394876.6:c.366T>G	ENSP00000378342.2:p.His122Gln
ENST00000394877.7:c.366T>G	ENSP00000378343.3:p.His122Gln
ENST00000455368.6:c.366T>G	ENSP00000397551.2:p.His122Gln
ENST00000514547.1:c.366T>G	ENSP00000423628.1:p.His122Gln
ENST00000515831.1:n.132T>G
NM_001134665.2:c.366T>G	NP_001128137.1:p.His122Gln
NM_001134666.2:c.366T>G	NP_001128138.1:p.His122Gln
NM_152292.4:c.366T>G	NP_689505.1:p.His122Gln
XM_005263352.3:c.366T>G	XP_005263409.1:p.His122Gln
XM_006714417.2:c.366T>G	XP_006714480.1:p.His122Gln
XM_006714418.2:c.366T>G	XP_006714481.1:p.His122Gln
NM_001134665.3:c.366T>G MANE Select	NP_001128137.1:p.His122Gln
NM_001134666.3:c.366T>G	NP_001128138.1:p.His122Gln
NM_001375880.1:c.366T>G	NP_001362809.1:p.His122Gln
NM_001375881.1:c.366T>G	NP_001362810.1:p.His122Gln
NM_001375882.1:c.366T>G	NP_001362811.1:p.His122Gln
NM_152292.5:c.366T>G	NP_689505.1:p.His122Gln