Canonical Allele Identifier: CA357510827

Gene: TRMT10A

Linked Data

• MyVariant Identifiers: chr4:g.100478544T>A (hg19) ; chr4:g.99557387T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99557387T>A , CM000666.2:g.99557387T>A	GRCh38
NC_000004.11:g.100478544T>A , CM000666.1:g.100478544T>A	GRCh37
NC_000004.10:g.100697567T>A	NCBI36
NG_041774.1:g.11671A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000394876.7:c.378A>T MANE Select	ENSP00000378342.2:p.Gln126His
ENST00000273962.7:c.378A>T	ENSP00000273962.3:p.Gln126His
ENST00000394876.6:c.378A>T	ENSP00000378342.2:p.Gln126His
ENST00000394877.7:c.378A>T	ENSP00000378343.3:p.Gln126His
ENST00000455368.6:c.378A>T	ENSP00000397551.2:p.Gln126His
ENST00000514547.1:c.378A>T	ENSP00000423628.1:p.Gln126His
ENST00000515831.1:n.144A>T
NM_001134665.2:c.378A>T	NP_001128137.1:p.Gln126His
NM_001134666.2:c.378A>T	NP_001128138.1:p.Gln126His
NM_152292.4:c.378A>T	NP_689505.1:p.Gln126His
XM_005263352.3:c.378A>T	XP_005263409.1:p.Gln126His
XM_006714417.2:c.378A>T	XP_006714480.1:p.Gln126His
XM_006714418.2:c.378A>T	XP_006714481.1:p.Gln126His
NM_001134665.3:c.378A>T MANE Select	NP_001128137.1:p.Gln126His
NM_001134666.3:c.378A>T	NP_001128138.1:p.Gln126His
NM_001375880.1:c.378A>T	NP_001362809.1:p.Gln126His
NM_001375881.1:c.378A>T	NP_001362810.1:p.Gln126His
NM_001375882.1:c.378A>T	NP_001362811.1:p.Gln126His
NM_152292.5:c.378A>T	NP_689505.1:p.Gln126His