Canonical Allele Identifier: CA2645075265

Gene: TRIT1

Linked Data

• gnomAD v4: 1-39847052-C-CTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.39847052_39847053insTTT , CM000663.2:g.39847052_39847053insTTT	GRCh38
NC_000001.10:g.40312724_40312725insTTT , CM000663.1:g.40312724_40312725insTTT	GRCh37
NC_000001.9:g.40085311_40085312insTTT	NCBI36
NG_042822.1:g.41459_41460insAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316891.10:c.1006+167_1006+168insAAA MANE Select	ENSP00000321810.5:n.1006+167_1006+168insAAA
ENST00000648678.1:c.1898+167_1898+168insAAA	ENSP00000497805.1:n.1898+167_1898+168insAAA
ENST00000316891.9:c.1006+167_1006+168insAAA	ENSP00000321810.5:n.1006+167_1006+168insAAA
ENST00000372818.5:c.928+495_928+496insAAA	ENSP00000361905.1:n.928+495_928+496insAAA
ENST00000441669.6:c.760+167_760+168insAAA	ENSP00000388333.2:n.760+167_760+168insAAA
ENST00000462797.5:c.1006+167_1006+168insAAA	ENSP00000473773.1:n.1006+167_1006+168insAAA
ENST00000465417.5:n.190+167_190+168insAAA
ENST00000467774.1:n.455_456insAAA
ENST00000491865.5:n.241+167_241+168insAAA
ENST00000492612.6:c.850+167_850+168insAAA
ENST00000495175.6:c.*428+167_*428+168insAAA	ENSP00000474264.1:n.*428+167_*428+168insAAA
ENST00000537440.5:c.94+167_94+168insAAA	ENSP00000437700.1:n.94+167_94+168insAAA
ENST00000541099.5:c.-140-2413_-140-2412insAAA	ENSP00000437896.1:n.-140-2413_-140-2412insAAA
NM_001312691.1:c.928+495_928+496insAAA	NP_001299620.1:n.928+495_928+496insAAA
NM_001312692.1:c.760+167_760+168insAAA	NP_001299621.1:n.760+167_760+168insAAA
NM_017646.4:c.1006+167_1006+168insAAA	NP_060116.2:n.1006+167_1006+168insAAA
NM_017646.5:c.1006+167_1006+168insAAA	NP_060116.2:n.1006+167_1006+168insAAA
NR_132401.1:n.1022+167_1022+168insAAA
NR_132402.1:n.880+167_880+168insAAA
NR_132403.1:n.876+167_876+168insAAA
NR_132404.1:n.876+167_876+168insAAA
NR_132405.1:n.872+167_872+168insAAA
NR_132406.1:n.763+167_763+168insAAA
NR_132407.1:n.640+167_640+168insAAA
NR_132408.1:n.636+167_636+168insAAA
NR_132409.1:n.497+167_497+168insAAA
NR_132410.1:n.523+167_523+168insAAA
NR_132412.1:n.384+167_384+168insAAA
NR_132413.1:n.195-2413_195-2412insAAA
NR_132414.1:n.195-5140_195-5139insAAA
NR_132415.1:n.1113+167_1113+168insAAA
XM_005270954.1:c.763+167_763+168insAAA	XP_005271011.1:n.763+167_763+168insAAA
XM_006710706.1:c.583+167_583+168insAAA	XP_006710769.1:n.583+167_583+168insAAA
XM_005270954.2:c.763+167_763+168insAAA	XP_005271011.1:n.763+167_763+168insAAA
XR_946672.2:n.1106+167_1106+168insAAA
NM_017646.6:c.1006+167_1006+168insAAA MANE Select	NP_060116.2:n.1006+167_1006+168insAAA