Canonical Allele Identifier: CA440335268

Gene: TRMT10A

Linked Data

• MyVariant Identifiers: chr4:g.100478514C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99557357C>A , CM000666.2:g.99557357C>A	GRCh38
NC_000004.11:g.100478514C>A , CM000666.1:g.100478514C>A	GRCh37
NC_000004.10:g.100697537C>A	NCBI36
NG_041774.1:g.11701G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394876.7:c.408G>T MANE Select	ENSP00000378342.2:p.Leu136=
ENST00000273962.7:c.408G>T	ENSP00000273962.3:p.Leu136=
ENST00000394876.6:c.408G>T	ENSP00000378342.2:p.Leu136=
ENST00000394877.7:c.408G>T	ENSP00000378343.3:p.Leu136=
ENST00000455368.6:c.408G>T	ENSP00000397551.2:p.Leu136=
ENST00000514547.1:c.408G>T	ENSP00000423628.1:p.Leu136=
ENST00000515831.1:n.174G>T
NM_001134665.2:c.408G>T	NP_001128137.1:p.Leu136=
NM_001134666.2:c.408G>T	NP_001128138.1:p.Leu136=
NM_152292.4:c.408G>T	NP_689505.1:p.Leu136=
XM_005263352.3:c.408G>T	XP_005263409.1:p.Leu136=
XM_006714417.2:c.408G>T	XP_006714480.1:p.Leu136=
XM_006714418.2:c.408G>T	XP_006714481.1:p.Leu136=
NM_001134665.3:c.408G>T MANE Select	NP_001128137.1:p.Leu136=
NM_001134666.3:c.408G>T	NP_001128138.1:p.Leu136=
NM_001375880.1:c.408G>T	NP_001362809.1:p.Leu136=
NM_001375881.1:c.408G>T	NP_001362810.1:p.Leu136=
NM_001375882.1:c.408G>T	NP_001362811.1:p.Leu136=
NM_152292.5:c.408G>T	NP_689505.1:p.Leu136=