Canonical Allele Identifier: CA2582798791

Gene: TRMT1

Linked Data

• gnomAD v4: 19-13110308-TGGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.13110311_13110313del , CM000681.2:g.13110311_13110313del	GRCh38
NC_000019.9:g.13221125_13221127del , CM000681.1:g.13221125_13221127del	GRCh37
NC_000019.8:g.13082125_13082127del	NCBI36
NG_054900.1:g.12257_12259del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357720.9:c.871-5_871-3del MANE Select	ENSP00000350352.4:n.871-5_871-3del
ENST00000221504.12:c.871-5_871-3del	ENSP00000221504.7:n.871-5_871-3del
ENST00000357720.8:c.871-5_871-3del	ENSP00000350352.4:n.871-5_871-3del
ENST00000437766.5:c.871-5_871-3del	ENSP00000416149.1:n.871-5_871-3del
ENST00000587487.5:c.229-5_229-3del	ENSP00000465370.1:n.229-5_229-3del
ENST00000587633.1:c.528-5_528-3del	ENSP00000466716.1:n.528-5_528-3del
ENST00000588511.5:n.1056-5_1056-3del
ENST00000592062.5:c.871-5_871-3del	ENSP00000466967.1:n.871-5_871-3del
ENST00000592814.5:c.745-5_745-3del	ENSP00000467938.1:n.745-5_745-3del
ENST00000593157.5:n.900-5_900-3del
NM_001136035.2:c.871-5_871-3del	NP_001129507.1:n.871-5_871-3del
NM_001142554.1:c.871-5_871-3del	NP_001136026.1:n.871-5_871-3del
NM_017722.3:c.871-5_871-3del	NP_060192.1:n.871-5_871-3del
XM_005259983.1:c.871-5_871-3del	XP_005260040.1:n.871-5_871-3del
XM_006722793.2:c.229-5_229-3del	XP_006722856.1:n.229-5_229-3del
XM_011528124.1:c.763-5_763-3del	XP_011526426.1:n.763-5_763-3del
XM_011528125.1:c.229-5_229-3del	XP_011526427.1:n.229-5_229-3del
XM_011528126.1:c.88-5_88-3del	XP_011526428.1:n.88-5_88-3del
NM_001136035.3:c.871-5_871-3del	NP_001129507.1:n.871-5_871-3del
NM_001142554.2:c.871-5_871-3del	NP_001136026.1:n.871-5_871-3del
NM_001351760.1:c.871-5_871-3del	NP_001338689.1:n.871-5_871-3del
NM_001351761.1:c.763-5_763-3del	NP_001338690.1:n.763-5_763-3del
NM_001351762.1:c.88-5_88-3del	NP_001338691.1:n.88-5_88-3del
NM_017722.4:c.871-5_871-3del	NP_060192.1:n.871-5_871-3del
XM_024451587.1:c.229-5_229-3del	XP_024307355.1:n.229-5_229-3del
XM_024451588.1:c.229-5_229-3del	XP_024307356.1:n.229-5_229-3del
XM_024451589.1:c.229-5_229-3del	XP_024307357.1:n.229-5_229-3del
XM_024451590.1:c.229-5_229-3del	XP_024307358.1:n.229-5_229-3del
XM_024451591.1:c.88-5_88-3del	XP_024307359.1:n.88-5_88-3del
XM_024451592.1:c.88-5_88-3del	XP_024307360.1:n.88-5_88-3del
XM_024451593.1:c.88-5_88-3del	XP_024307361.1:n.88-5_88-3del
XR_002958328.1:n.997-5_997-3del
XR_002958329.1:n.696-5_696-3del
NM_001136035.4:c.871-5_871-3del MANE Select	NP_001129507.1:n.871-5_871-3del
NM_001142554.3:c.871-5_871-3del	NP_001136026.1:n.871-5_871-3del
NM_001351760.2:c.871-5_871-3del	NP_001338689.1:n.871-5_871-3del
NM_001351761.2:c.763-5_763-3del	NP_001338690.1:n.763-5_763-3del
NM_001351762.2:c.88-5_88-3del	NP_001338691.1:n.88-5_88-3del
NM_017722.5:c.871-5_871-3del	NP_060192.1:n.871-5_871-3del