Canonical Allele Identifier: CA2582798785

Gene: TRMT1

Linked Data

• gnomAD v4: 19-13110306-C-CGA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.13110306_13110307insGA , CM000681.2:g.13110306_13110307insGA	GRCh38
NC_000019.9:g.13221120_13221121insGA , CM000681.1:g.13221120_13221121insGA	GRCh37
NC_000019.8:g.13082120_13082121insGA	NCBI36
NG_054900.1:g.12261_12262insTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357720.9:c.871-1_871insTC MANE Select	ENSP00000350352.4:n.871-1_871insTC
ENST00000221504.12:c.871-1_871insTC	ENSP00000221504.7:n.871-1_871insTC
ENST00000357720.8:c.871-1_871insTC	ENSP00000350352.4:n.871-1_871insTC
ENST00000437766.5:c.871-1_871insTC	ENSP00000416149.1:n.871-1_871insTC
ENST00000587487.5:c.229-1_229insTC	ENSP00000465370.1:n.229-1_229insTC
ENST00000587633.1:c.528-1_528insTC	ENSP00000466716.1:n.528-1_528insTC
ENST00000588511.5:n.1056-1_1056insTC
ENST00000592062.5:c.871-1_871insTC	ENSP00000466967.1:n.871-1_871insTC
ENST00000592814.5:c.745-1_745insTC	ENSP00000467938.1:n.745-1_745insTC
ENST00000593157.5:n.900-1_900insTC
NM_001136035.2:c.871-1_871insTC	NP_001129507.1:n.871-1_871insTC
NM_001142554.1:c.871-1_871insTC	NP_001136026.1:n.871-1_871insTC
NM_017722.3:c.871-1_871insTC	NP_060192.1:n.871-1_871insTC
XM_005259983.1:c.871-1_871insTC	XP_005260040.1:n.871-1_871insTC
XM_006722793.2:c.229-1_229insTC	XP_006722856.1:n.229-1_229insTC
XM_011528124.1:c.763-1_763insTC	XP_011526426.1:n.763-1_763insTC
XM_011528125.1:c.229-1_229insTC	XP_011526427.1:n.229-1_229insTC
XM_011528126.1:c.88-1_88insTC	XP_011526428.1:n.88-1_88insTC
NM_001136035.3:c.871-1_871insTC	NP_001129507.1:n.871-1_871insTC
NM_001142554.2:c.871-1_871insTC	NP_001136026.1:n.871-1_871insTC
NM_001351760.1:c.871-1_871insTC	NP_001338689.1:n.871-1_871insTC
NM_001351761.1:c.763-1_763insTC	NP_001338690.1:n.763-1_763insTC
NM_001351762.1:c.88-1_88insTC	NP_001338691.1:n.88-1_88insTC
NM_017722.4:c.871-1_871insTC	NP_060192.1:n.871-1_871insTC
XM_024451587.1:c.229-1_229insTC	XP_024307355.1:n.229-1_229insTC
XM_024451588.1:c.229-1_229insTC	XP_024307356.1:n.229-1_229insTC
XM_024451589.1:c.229-1_229insTC	XP_024307357.1:n.229-1_229insTC
XM_024451590.1:c.229-1_229insTC	XP_024307358.1:n.229-1_229insTC
XM_024451591.1:c.88-1_88insTC	XP_024307359.1:n.88-1_88insTC
XM_024451592.1:c.88-1_88insTC	XP_024307360.1:n.88-1_88insTC
XM_024451593.1:c.88-1_88insTC	XP_024307361.1:n.88-1_88insTC
XR_002958328.1:n.997-1_997insTC
XR_002958329.1:n.696-1_696insTC
NM_001136035.4:c.871-1_871insTC MANE Select	NP_001129507.1:n.871-1_871insTC
NM_001142554.3:c.871-1_871insTC	NP_001136026.1:n.871-1_871insTC
NM_001351760.2:c.871-1_871insTC	NP_001338689.1:n.871-1_871insTC
NM_001351761.2:c.763-1_763insTC	NP_001338690.1:n.763-1_763insTC
NM_001351762.2:c.88-1_88insTC	NP_001338691.1:n.88-1_88insTC
NM_017722.5:c.871-1_871insTC	NP_060192.1:n.871-1_871insTC