Canonical Allele Identifier: CA2645075237

Gene: TRIT1

Linked Data

• gnomAD v4: 1-39847029-AAT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.39847030_39847031del , CM000663.2:g.39847030_39847031del	GRCh38
NC_000001.10:g.40312702_40312703del , CM000663.1:g.40312702_40312703del	GRCh37
NC_000001.9:g.40085289_40085290del	NCBI36
NG_042822.1:g.41481_41482del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316891.10:c.1006+189_1006+190del MANE Select	ENSP00000321810.5:n.1006+189_1006+190del
ENST00000648678.1:c.1898+189_1898+190del	ENSP00000497805.1:n.1898+189_1898+190del
ENST00000316891.9:c.1006+189_1006+190del	ENSP00000321810.5:n.1006+189_1006+190del
ENST00000372818.5:c.928+517_928+518del	ENSP00000361905.1:n.928+517_928+518del
ENST00000441669.6:c.760+189_760+190del	ENSP00000388333.2:n.760+189_760+190del
ENST00000462797.5:c.1006+189_1006+190del	ENSP00000473773.1:n.1006+189_1006+190del
ENST00000465417.5:n.190+189_190+190del
ENST00000491865.5:n.241+189_241+190del
ENST00000492612.6:c.850+189_850+190del
ENST00000495175.6:c.*428+189_*428+190del	ENSP00000474264.1:n.*428+189_*428+190del
ENST00000537440.5:c.94+189_94+190del	ENSP00000437700.1:n.94+189_94+190del
ENST00000541099.5:c.-140-2391_-140-2390del	ENSP00000437896.1:n.-140-2391_-140-2390del
NM_001312691.1:c.928+517_928+518del	NP_001299620.1:n.928+517_928+518del
NM_001312692.1:c.760+189_760+190del	NP_001299621.1:n.760+189_760+190del
NM_017646.4:c.1006+189_1006+190del	NP_060116.2:n.1006+189_1006+190del
NM_017646.5:c.1006+189_1006+190del	NP_060116.2:n.1006+189_1006+190del
NR_132401.1:n.1022+189_1022+190del
NR_132402.1:n.880+189_880+190del
NR_132403.1:n.876+189_876+190del
NR_132404.1:n.876+189_876+190del
NR_132405.1:n.872+189_872+190del
NR_132406.1:n.763+189_763+190del
NR_132407.1:n.640+189_640+190del
NR_132408.1:n.636+189_636+190del
NR_132409.1:n.497+189_497+190del
NR_132410.1:n.523+189_523+190del
NR_132412.1:n.384+189_384+190del
NR_132413.1:n.195-2391_195-2390del
NR_132414.1:n.195-5118_195-5117del
NR_132415.1:n.1113+189_1113+190del
XM_005270954.1:c.763+189_763+190del	XP_005271011.1:n.763+189_763+190del
XM_006710706.1:c.583+189_583+190del	XP_006710769.1:n.583+189_583+190del
XM_005270954.2:c.763+189_763+190del	XP_005271011.1:n.763+189_763+190del
XR_946672.2:n.1106+189_1106+190del
NM_017646.6:c.1006+189_1006+190del MANE Select	NP_060116.2:n.1006+189_1006+190del