Canonical Allele Identifier: CA800729649

Gene: TRMT10A

Linked Data

• dbSNP Id: rs1188305323
• gnomAD v4: 4-99557286-CT-C
• MyVariant Identifiers: chr4:g.100478444del (hg19) ; chr4:g.99557287del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99557290del , CM000666.2:g.99557290del	GRCh38
NC_000004.11:g.100478447del , CM000666.1:g.100478447del	GRCh37
NC_000004.10:g.100697470del	NCBI36
NG_041774.1:g.11771del

Transcript Alleles

HGVS	Amino-acid change
ENST00000394876.7:c.420+58del MANE Select	ENSP00000378342.2:n.420+58del
ENST00000273962.7:c.420+58del	ENSP00000273962.3:n.420+58del
ENST00000394876.6:c.420+58del	ENSP00000378342.2:n.420+58del
ENST00000394877.7:c.420+58del	ENSP00000378343.3:n.420+58del
ENST00000455368.6:c.420+58del	ENSP00000397551.2:n.420+58del
ENST00000514547.1:c.420+58del	ENSP00000423628.1:n.420+58del
ENST00000515831.1:n.186+58del
NM_001134665.2:c.420+58del	NP_001128137.1:n.420+58del
NM_001134666.2:c.420+58del	NP_001128138.1:n.420+58del
NM_152292.4:c.420+58del	NP_689505.1:n.420+58del
XM_005263352.3:c.420+58del	XP_005263409.1:n.420+58del
XM_006714417.2:c.420+58del	XP_006714480.1:n.420+58del
XM_006714418.2:c.420+58del	XP_006714481.1:n.420+58del
NM_001134665.3:c.420+58del MANE Select	NP_001128137.1:n.420+58del
NM_001134666.3:c.420+58del	NP_001128138.1:n.420+58del
NM_001375880.1:c.420+58del	NP_001362809.1:n.420+58del
NM_001375881.1:c.420+58del	NP_001362810.1:n.420+58del
NM_001375882.1:c.420+58del	NP_001362811.1:n.420+58del
NM_152292.5:c.420+58del	NP_689505.1:n.420+58del