Canonical Allele Identifier: CA2582798729

Gene: TRMT1

Linked Data

• gnomAD v4: 19-13110037-T-TGACCACGACACCCCAACTCCTCCCTTAGACTG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.13110039_13110070dup , CM000681.2:g.13110039_13110070dup	GRCh38
NC_000019.9:g.13220853_13220884dup , CM000681.1:g.13220853_13220884dup	GRCh37
NC_000019.8:g.13081853_13081884dup	NCBI36
NG_054900.1:g.12499_12530dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357720.9:c.1020-68_1020-37dup MANE Select	ENSP00000350352.4:n.1020-68_1020-37dup
ENST00000221504.12:c.1019+89_1019+120dup	ENSP00000221504.7:n.1019+89_1019+120dup
ENST00000357720.8:c.1020-68_1020-37dup	ENSP00000350352.4:n.1020-68_1020-37dup
ENST00000437766.5:c.1020-68_1020-37dup	ENSP00000416149.1:n.1020-68_1020-37dup
ENST00000587487.5:c.378-68_378-37dup	ENSP00000465370.1:n.378-68_378-37dup
ENST00000588511.5:n.1205-68_1205-37dup
ENST00000592062.5:c.1020-68_1020-37dup	ENSP00000466967.1:n.1020-68_1020-37dup
ENST00000593157.5:n.1049-68_1049-37dup
NM_001136035.2:c.1020-68_1020-37dup	NP_001129507.1:n.1020-68_1020-37dup
NM_001142554.1:c.1019+89_1019+120dup	NP_001136026.1:n.1019+89_1019+120dup
NM_017722.3:c.1020-68_1020-37dup	NP_060192.1:n.1020-68_1020-37dup
XM_005259983.1:c.1019+89_1019+120dup	XP_005260040.1:n.1019+89_1019+120dup
XM_006722793.2:c.378-68_378-37dup	XP_006722856.1:n.378-68_378-37dup
XM_011528124.1:c.912-68_912-37dup	XP_011526426.1:n.912-68_912-37dup
XM_011528125.1:c.378-68_378-37dup	XP_011526427.1:n.378-68_378-37dup
XM_011528126.1:c.237-68_237-37dup	XP_011526428.1:n.237-68_237-37dup
NM_001136035.3:c.1020-68_1020-37dup	NP_001129507.1:n.1020-68_1020-37dup
NM_001142554.2:c.1019+89_1019+120dup	NP_001136026.1:n.1019+89_1019+120dup
NM_001351760.1:c.1019+89_1019+120dup	NP_001338689.1:n.1019+89_1019+120dup
NM_001351761.1:c.912-68_912-37dup	NP_001338690.1:n.912-68_912-37dup
NM_001351762.1:c.237-68_237-37dup	NP_001338691.1:n.237-68_237-37dup
NM_017722.4:c.1020-68_1020-37dup	NP_060192.1:n.1020-68_1020-37dup
XM_024451587.1:c.378-68_378-37dup	XP_024307355.1:n.378-68_378-37dup
XM_024451588.1:c.378-68_378-37dup	XP_024307356.1:n.378-68_378-37dup
XM_024451589.1:c.378-68_378-37dup	XP_024307357.1:n.378-68_378-37dup
XM_024451590.1:c.377+89_377+120dup	XP_024307358.1:n.377+89_377+120dup
XM_024451591.1:c.237-68_237-37dup	XP_024307359.1:n.237-68_237-37dup
XM_024451592.1:c.237-68_237-37dup	XP_024307360.1:n.237-68_237-37dup
XM_024451593.1:c.237-68_237-37dup	XP_024307361.1:n.237-68_237-37dup
XR_002958328.1:n.1145+89_1145+120dup
XR_002958329.1:n.844+89_844+120dup
NM_001136035.4:c.1020-68_1020-37dup MANE Select	NP_001129507.1:n.1020-68_1020-37dup
NM_001142554.3:c.1019+89_1019+120dup	NP_001136026.1:n.1019+89_1019+120dup
NM_001351760.2:c.1019+89_1019+120dup	NP_001338689.1:n.1019+89_1019+120dup
NM_001351761.2:c.912-68_912-37dup	NP_001338690.1:n.912-68_912-37dup
NM_001351762.2:c.237-68_237-37dup	NP_001338691.1:n.237-68_237-37dup
NM_017722.5:c.1020-68_1020-37dup	NP_060192.1:n.1020-68_1020-37dup