Canonical Allele Identifier: CA1000849881

Gene: TRIT1

Linked Data

• gnomAD v3: 1-39847046-TGACA-T
• gnomAD v4: 1-39847046-TGACA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.39847047_39847050del , CM000663.2:g.39847047_39847050del	GRCh38
NC_000001.10:g.40312719_40312722del , CM000663.1:g.40312719_40312722del	GRCh37
NC_000001.9:g.40085306_40085309del	NCBI36
NG_042822.1:g.41462_41465del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316891.10:c.1006+170_1006+173del MANE Select	ENSP00000321810.5:n.1006+170_1006+173del
ENST00000648678.1:c.1898+170_1898+173del	ENSP00000497805.1:n.1898+170_1898+173del
ENST00000316891.9:c.1006+170_1006+173del	ENSP00000321810.5:n.1006+170_1006+173del
ENST00000372818.5:c.928+498_928+501del	ENSP00000361905.1:n.928+498_928+501del
ENST00000441669.6:c.760+170_760+173del	ENSP00000388333.2:n.760+170_760+173del
ENST00000462797.5:c.1006+170_1006+173del	ENSP00000473773.1:n.1006+170_1006+173del
ENST00000465417.5:n.190+170_190+173del
ENST00000467774.1:n.458_461del
ENST00000491865.5:n.241+170_241+173del
ENST00000492612.6:c.850+170_850+173del
ENST00000495175.6:c.*428+170_*428+173del	ENSP00000474264.1:n.*428+170_*428+173del
ENST00000537440.5:c.94+170_94+173del	ENSP00000437700.1:n.94+170_94+173del
ENST00000541099.5:c.-140-2410_-140-2407del	ENSP00000437896.1:n.-140-2410_-140-2407del
NM_001312691.1:c.928+498_928+501del	NP_001299620.1:n.928+498_928+501del
NM_001312692.1:c.760+170_760+173del	NP_001299621.1:n.760+170_760+173del
NM_017646.4:c.1006+170_1006+173del	NP_060116.2:n.1006+170_1006+173del
NM_017646.5:c.1006+170_1006+173del	NP_060116.2:n.1006+170_1006+173del
NR_132401.1:n.1022+170_1022+173del
NR_132402.1:n.880+170_880+173del
NR_132403.1:n.876+170_876+173del
NR_132404.1:n.876+170_876+173del
NR_132405.1:n.872+170_872+173del
NR_132406.1:n.763+170_763+173del
NR_132407.1:n.640+170_640+173del
NR_132408.1:n.636+170_636+173del
NR_132409.1:n.497+170_497+173del
NR_132410.1:n.523+170_523+173del
NR_132412.1:n.384+170_384+173del
NR_132413.1:n.195-2410_195-2407del
NR_132414.1:n.195-5137_195-5134del
NR_132415.1:n.1113+170_1113+173del
XM_005270954.1:c.763+170_763+173del	XP_005271011.1:n.763+170_763+173del
XM_006710706.1:c.583+170_583+173del	XP_006710769.1:n.583+170_583+173del
XM_005270954.2:c.763+170_763+173del	XP_005271011.1:n.763+170_763+173del
XR_946672.2:n.1106+170_1106+173del
NM_017646.6:c.1006+170_1006+173del MANE Select	NP_060116.2:n.1006+170_1006+173del