Canonical Allele Identifier: CA2645075371

Gene: TRIT1

Linked Data

• gnomAD v4: 1-39847306-TAC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.39847308_39847309del , CM000663.2:g.39847308_39847309del	GRCh38
NC_000001.10:g.40312980_40312981del , CM000663.1:g.40312980_40312981del	GRCh37
NC_000001.9:g.40085567_40085568del	NCBI36
NG_042822.1:g.41204_41205del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316891.10:c.929-11_929-10del MANE Select	ENSP00000321810.5:n.929-11_929-10del
ENST00000648678.1:c.1821-11_1821-10del	ENSP00000497805.1:n.1821-11_1821-10del
ENST00000316891.9:c.929-11_929-10del	ENSP00000321810.5:n.929-11_929-10del
ENST00000372818.5:c.928+240_928+241del	ENSP00000361905.1:n.928+240_928+241del
ENST00000441669.6:c.683-11_683-10del	ENSP00000388333.2:n.683-11_683-10del
ENST00000462797.5:c.929-11_929-10del	ENSP00000473773.1:n.929-11_929-10del
ENST00000465417.5:n.113-11_113-10del
ENST00000467774.1:n.211-11_211-10del
ENST00000486825.6:c.834-11_834-10del
ENST00000489945.5:c.*347-11_*347-10del	ENSP00000473745.1:n.*347-11_*347-10del
ENST00000491865.5:n.164-11_164-10del
ENST00000492612.6:c.773-11_773-10del
ENST00000495175.6:c.*351-11_*351-10del	ENSP00000474264.1:n.*351-11_*351-10del
ENST00000537440.5:c.17-11_17-10del	ENSP00000437700.1:n.17-11_17-10del
ENST00000541099.5:c.-140-2668_-140-2667del	ENSP00000437896.1:n.-140-2668_-140-2667del
NM_001312691.1:c.928+240_928+241del	NP_001299620.1:n.928+240_928+241del
NM_001312692.1:c.683-11_683-10del	NP_001299621.1:n.683-11_683-10del
NM_017646.4:c.929-11_929-10del	NP_060116.2:n.929-11_929-10del
NM_017646.5:c.929-11_929-10del	NP_060116.2:n.929-11_929-10del
NR_132401.1:n.945-11_945-10del
NR_132402.1:n.803-11_803-10del
NR_132403.1:n.799-11_799-10del
NR_132404.1:n.799-11_799-10del
NR_132405.1:n.795-11_795-10del
NR_132406.1:n.686-11_686-10del
NR_132407.1:n.563-11_563-10del
NR_132408.1:n.559-11_559-10del
NR_132409.1:n.420-11_420-10del
NR_132410.1:n.446-11_446-10del
NR_132412.1:n.307-11_307-10del
NR_132413.1:n.195-2668_195-2667del
NR_132414.1:n.195-5395_195-5394del
NR_132415.1:n.1036-11_1036-10del
XM_005270954.1:c.686-11_686-10del	XP_005271011.1:n.686-11_686-10del
XM_006710706.1:c.506-11_506-10del	XP_006710769.1:n.506-11_506-10del
XM_005270954.2:c.686-11_686-10del	XP_005271011.1:n.686-11_686-10del
XR_946672.2:n.1029-11_1029-10del
NM_017646.6:c.929-11_929-10del MANE Select	NP_060116.2:n.929-11_929-10del