Canonical Allele Identifier: CA2645075412

Gene: TRIT1

Linked Data

• gnomAD v4: 1-39847378-GAA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.39847382_39847383del , CM000663.2:g.39847382_39847383del	GRCh38
NC_000001.10:g.40313054_40313055del , CM000663.1:g.40313054_40313055del	GRCh37
NC_000001.9:g.40085641_40085642del	NCBI36
NG_042822.1:g.41132_41133del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316891.10:c.929-83_929-82del MANE Select	ENSP00000321810.5:n.929-83_929-82del
ENST00000648678.1:c.1821-83_1821-82del	ENSP00000497805.1:n.1821-83_1821-82del
ENST00000316891.9:c.929-83_929-82del	ENSP00000321810.5:n.929-83_929-82del
ENST00000372818.5:c.928+168_928+169del	ENSP00000361905.1:n.928+168_928+169del
ENST00000441669.6:c.683-83_683-82del	ENSP00000388333.2:n.683-83_683-82del
ENST00000462797.5:c.929-83_929-82del	ENSP00000473773.1:n.929-83_929-82del
ENST00000465417.5:n.113-83_113-82del
ENST00000467774.1:n.211-83_211-82del
ENST00000486825.6:c.834-83_834-82del
ENST00000489945.5:c.*347-83_*347-82del	ENSP00000473745.1:n.*347-83_*347-82del
ENST00000491865.5:n.164-83_164-82del
ENST00000492612.6:c.773-83_773-82del
ENST00000495175.6:c.*351-83_*351-82del	ENSP00000474264.1:n.*351-83_*351-82del
ENST00000537440.5:c.17-83_17-82del	ENSP00000437700.1:n.17-83_17-82del
ENST00000541099.5:c.-140-2740_-140-2739del	ENSP00000437896.1:n.-140-2740_-140-2739del
NM_001312691.1:c.928+168_928+169del	NP_001299620.1:n.928+168_928+169del
NM_001312692.1:c.683-83_683-82del	NP_001299621.1:n.683-83_683-82del
NM_017646.4:c.929-83_929-82del	NP_060116.2:n.929-83_929-82del
NM_017646.5:c.929-83_929-82del	NP_060116.2:n.929-83_929-82del
NR_132401.1:n.945-83_945-82del
NR_132402.1:n.803-83_803-82del
NR_132403.1:n.799-83_799-82del
NR_132404.1:n.799-83_799-82del
NR_132405.1:n.795-83_795-82del
NR_132406.1:n.686-83_686-82del
NR_132407.1:n.563-83_563-82del
NR_132408.1:n.559-83_559-82del
NR_132409.1:n.420-83_420-82del
NR_132410.1:n.446-83_446-82del
NR_132412.1:n.307-83_307-82del
NR_132413.1:n.195-2740_195-2739del
NR_132414.1:n.195-5467_195-5466del
NR_132415.1:n.1036-83_1036-82del
XM_005270954.1:c.686-83_686-82del	XP_005271011.1:n.686-83_686-82del
XM_006710706.1:c.506-83_506-82del	XP_006710769.1:n.506-83_506-82del
XM_005270954.2:c.686-83_686-82del	XP_005271011.1:n.686-83_686-82del
XR_946672.2:n.1029-83_1029-82del
NM_017646.6:c.929-83_929-82del MANE Select	NP_060116.2:n.929-83_929-82del