Canonical Allele Identifier: CA2645075390

Gene: TRIT1

Linked Data

• gnomAD v4: 1-39847349-C-CCTCTCTGCAGGGT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.39847349_39847350insCTCTCTGCAGGGT , CM000663.2:g.39847349_39847350insCTCTCTGCAGGGT	GRCh38
NC_000001.10:g.40313021_40313022insCTCTCTGCAGGGT , CM000663.1:g.40313021_40313022insCTCTCTGCAGGGT	GRCh37
NC_000001.9:g.40085608_40085609insCTCTCTGCAGGGT	NCBI36
NG_042822.1:g.41162_41163insACCCTGCAGAGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316891.10:c.929-53_929-52insACCCTGCAGAGAG MANE Select	ENSP00000321810.5:n.929-53_929-52insACCCTGCAGAGAG
ENST00000648678.1:c.1821-53_1821-52insACCCTGCAGAGAG	ENSP00000497805.1:n.1821-53_1821-52insACCCTGCAGAGAG
ENST00000316891.9:c.929-53_929-52insACCCTGCAGAGAG	ENSP00000321810.5:n.929-53_929-52insACCCTGCAGAGAG
ENST00000372818.5:c.928+198_928+199insACCCTGCAGAGAG	ENSP00000361905.1:n.928+198_928+199insACCCTGCAGAGAG
ENST00000441669.6:c.683-53_683-52insACCCTGCAGAGAG	ENSP00000388333.2:n.683-53_683-52insACCCTGCAGAGAG
ENST00000462797.5:c.929-53_929-52insACCCTGCAGAGAG	ENSP00000473773.1:n.929-53_929-52insACCCTGCAGAGAG
ENST00000465417.5:n.113-53_113-52insACCCTGCAGAGAG
ENST00000467774.1:n.211-53_211-52insACCCTGCAGAGAG
ENST00000486825.6:c.834-53_834-52insACCCTGCAGAGAG
ENST00000489945.5:c.*347-53_*347-52insACCCTGCAGAGAG	ENSP00000473745.1:n.*347-53_*347-52insACCCTGCAGAGAG
ENST00000491865.5:n.164-53_164-52insACCCTGCAGAGAG
ENST00000492612.6:c.773-53_773-52insACCCTGCAGAGAG
ENST00000495175.6:c.*351-53_*351-52insACCCTGCAGAGAG	ENSP00000474264.1:n.*351-53_*351-52insACCCTGCAGAGAG
ENST00000537440.5:c.17-53_17-52insACCCTGCAGAGAG	ENSP00000437700.1:n.17-53_17-52insACCCTGCAGAGAG
ENST00000541099.5:c.-140-2710_-140-2709insACCCTGCAGAGAG	ENSP00000437896.1:n.-140-2710_-140-2709insACCCTGCAGAGAG
NM_001312691.1:c.928+198_928+199insACCCTGCAGAGAG	NP_001299620.1:n.928+198_928+199insACCCTGCAGAGAG
NM_001312692.1:c.683-53_683-52insACCCTGCAGAGAG	NP_001299621.1:n.683-53_683-52insACCCTGCAGAGAG
NM_017646.4:c.929-53_929-52insACCCTGCAGAGAG	NP_060116.2:n.929-53_929-52insACCCTGCAGAGAG
NM_017646.5:c.929-53_929-52insACCCTGCAGAGAG	NP_060116.2:n.929-53_929-52insACCCTGCAGAGAG
NR_132401.1:n.945-53_945-52insACCCTGCAGAGAG
NR_132402.1:n.803-53_803-52insACCCTGCAGAGAG
NR_132403.1:n.799-53_799-52insACCCTGCAGAGAG
NR_132404.1:n.799-53_799-52insACCCTGCAGAGAG
NR_132405.1:n.795-53_795-52insACCCTGCAGAGAG
NR_132406.1:n.686-53_686-52insACCCTGCAGAGAG
NR_132407.1:n.563-53_563-52insACCCTGCAGAGAG
NR_132408.1:n.559-53_559-52insACCCTGCAGAGAG
NR_132409.1:n.420-53_420-52insACCCTGCAGAGAG
NR_132410.1:n.446-53_446-52insACCCTGCAGAGAG
NR_132412.1:n.307-53_307-52insACCCTGCAGAGAG
NR_132413.1:n.195-2710_195-2709insACCCTGCAGAGAG
NR_132414.1:n.195-5437_195-5436insACCCTGCAGAGAG
NR_132415.1:n.1036-53_1036-52insACCCTGCAGAGAG
XM_005270954.1:c.686-53_686-52insACCCTGCAGAGAG	XP_005271011.1:n.686-53_686-52insACCCTGCAGAGAG
XM_006710706.1:c.506-53_506-52insACCCTGCAGAGAG	XP_006710769.1:n.506-53_506-52insACCCTGCAGAGAG
XM_005270954.2:c.686-53_686-52insACCCTGCAGAGAG	XP_005271011.1:n.686-53_686-52insACCCTGCAGAGAG
XR_946672.2:n.1029-53_1029-52insACCCTGCAGAGAG
NM_017646.6:c.929-53_929-52insACCCTGCAGAGAG MANE Select	NP_060116.2:n.929-53_929-52insACCCTGCAGAGAG