Canonical Allele Identifier: CA2743285360

Gene: TRIT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.39847540_39847541insC , CM000663.2:g.39847540_39847541insC	GRCh38
NC_000001.10:g.40313212_40313213insC , CM000663.1:g.40313212_40313213insC	GRCh37
NC_000001.9:g.40085799_40085800insC	NCBI36
NG_042822.1:g.40971_40972insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316891.10:c.928+7_928+8insG MANE Select	ENSP00000321810.5:n.928+7_928+8insG
ENST00000648678.1:c.1820+7_1820+8insG	ENSP00000497805.1:n.1820+7_1820+8insG
ENST00000316891.9:c.928+7_928+8insG	ENSP00000321810.5:n.928+7_928+8insG
ENST00000372818.5:c.928+7_928+8insG	ENSP00000361905.1:n.928+7_928+8insG
ENST00000441669.6:c.682+7_682+8insG	ENSP00000388333.2:n.682+7_682+8insG
ENST00000462797.5:c.928+7_928+8insG	ENSP00000473773.1:n.928+7_928+8insG
ENST00000465417.5:n.113-244_113-243insG
ENST00000467774.1:n.210+7_210+8insG
ENST00000486825.6:c.833+7_833+8insG
ENST00000489945.5:c.*346+7_*346+8insG	ENSP00000473745.1:n.*346+7_*346+8insG
ENST00000491865.5:n.164-244_164-243insG
ENST00000492612.6:c.772+7_772+8insG
ENST00000495175.6:c.*350+7_*350+8insG	ENSP00000474264.1:n.*350+7_*350+8insG
ENST00000537440.5:c.17-244_17-243insG	ENSP00000437700.1:n.17-244_17-243insG
ENST00000541099.5:c.-140-2901_-140-2900insG	ENSP00000437896.1:n.-140-2901_-140-2900insG
NM_001312691.1:c.928+7_928+8insG	NP_001299620.1:n.928+7_928+8insG
NM_001312692.1:c.682+7_682+8insG	NP_001299621.1:n.682+7_682+8insG
NM_017646.4:c.928+7_928+8insG	NP_060116.2:n.928+7_928+8insG
NM_017646.5:c.928+7_928+8insG	NP_060116.2:n.928+7_928+8insG
NR_132401.1:n.944+7_944+8insG
NR_132402.1:n.802+7_802+8insG
NR_132403.1:n.798+7_798+8insG
NR_132404.1:n.798+7_798+8insG
NR_132405.1:n.794+7_794+8insG
NR_132406.1:n.686-244_686-243insG
NR_132407.1:n.562+7_562+8insG
NR_132408.1:n.558+7_558+8insG
NR_132409.1:n.419+7_419+8insG
NR_132410.1:n.446-244_446-243insG
NR_132412.1:n.307-244_307-243insG
NR_132413.1:n.195-2901_195-2900insG
NR_132414.1:n.195-5628_195-5627insG
NR_132415.1:n.1035+7_1035+8insG
XM_005270954.1:c.685+7_685+8insG	XP_005271011.1:n.685+7_685+8insG
XM_006710706.1:c.505+7_505+8insG	XP_006710769.1:n.505+7_505+8insG
XM_005270954.2:c.685+7_685+8insG	XP_005271011.1:n.685+7_685+8insG
XR_946672.2:n.1028+7_1028+8insG
NM_017646.6:c.928+7_928+8insG MANE Select	NP_060116.2:n.928+7_928+8insG