Canonical Allele Identifier: CA916157896

Gene: TRIT1

Linked Data

• dbSNP Id: rs201289596

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.39847093_39847094insCCAGGCCTA , CM000663.2:g.39847093_39847094insCCAGGCCTA	GRCh38
NC_000001.10:g.40312765_40312766insCCAGGCCTA , CM000663.1:g.40312765_40312766insCCAGGCCTA	GRCh37
NC_000001.9:g.40085352_40085353insCCAGGCCTA	NCBI36
NG_042822.1:g.41418_41419insTAGGCCTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316891.10:c.1006+126_1006+127insTAGGCCTGG MANE Select	ENSP00000321810.5:n.1006+126_1006+127insTAGGCCTGG
ENST00000648678.1:c.1898+126_1898+127insTAGGCCTGG	ENSP00000497805.1:n.1898+126_1898+127insTAGGCCTGG
ENST00000316891.9:c.1006+126_1006+127insTAGGCCTGG	ENSP00000321810.5:n.1006+126_1006+127insTAGGCCTGG
ENST00000372818.5:c.928+454_928+455insTAGGCCTGG	ENSP00000361905.1:n.928+454_928+455insTAGGCCTGG
ENST00000441669.6:c.760+126_760+127insTAGGCCTGG	ENSP00000388333.2:n.760+126_760+127insTAGGCCTGG
ENST00000462797.5:c.1006+126_1006+127insTAGGCCTGG	ENSP00000473773.1:n.1006+126_1006+127insTAGGCCTGG
ENST00000465417.5:n.190+126_190+127insTAGGCCTGG
ENST00000467774.1:n.414_415insTAGGCCTGG
ENST00000491865.5:n.241+126_241+127insTAGGCCTGG
ENST00000492612.6:c.850+126_850+127insTAGGCCTGG
ENST00000495175.6:c.*428+126_*428+127insTAGGCCTGG	ENSP00000474264.1:n.*428+126_*428+127insTAGGCCTGG
ENST00000537440.5:c.94+126_94+127insTAGGCCTGG	ENSP00000437700.1:n.94+126_94+127insTAGGCCTGG
ENST00000541099.5:c.-140-2454_-140-2453insTAGGCCTGG	ENSP00000437896.1:n.-140-2454_-140-2453insTAGGCCTGG
NM_001312691.1:c.928+454_928+455insTAGGCCTGG	NP_001299620.1:n.928+454_928+455insTAGGCCTGG
NM_001312692.1:c.760+126_760+127insTAGGCCTGG	NP_001299621.1:n.760+126_760+127insTAGGCCTGG
NM_017646.4:c.1006+126_1006+127insTAGGCCTGG	NP_060116.2:n.1006+126_1006+127insTAGGCCTGG
NM_017646.5:c.1006+126_1006+127insTAGGCCTGG	NP_060116.2:n.1006+126_1006+127insTAGGCCTGG
NR_132401.1:n.1022+126_1022+127insTAGGCCTGG
NR_132402.1:n.880+126_880+127insTAGGCCTGG
NR_132403.1:n.876+126_876+127insTAGGCCTGG
NR_132404.1:n.876+126_876+127insTAGGCCTGG
NR_132405.1:n.872+126_872+127insTAGGCCTGG
NR_132406.1:n.763+126_763+127insTAGGCCTGG
NR_132407.1:n.640+126_640+127insTAGGCCTGG
NR_132408.1:n.636+126_636+127insTAGGCCTGG
NR_132409.1:n.497+126_497+127insTAGGCCTGG
NR_132410.1:n.523+126_523+127insTAGGCCTGG
NR_132412.1:n.384+126_384+127insTAGGCCTGG
NR_132413.1:n.195-2454_195-2453insTAGGCCTGG
NR_132414.1:n.195-5181_195-5180insTAGGCCTGG
NR_132415.1:n.1113+126_1113+127insTAGGCCTGG
XM_005270954.1:c.763+126_763+127insTAGGCCTGG	XP_005271011.1:n.763+126_763+127insTAGGCCTGG
XM_006710706.1:c.583+126_583+127insTAGGCCTGG	XP_006710769.1:n.583+126_583+127insTAGGCCTGG
XM_005270954.2:c.763+126_763+127insTAGGCCTGG	XP_005271011.1:n.763+126_763+127insTAGGCCTGG
XR_946672.2:n.1106+126_1106+127insTAGGCCTGG
NM_017646.6:c.1006+126_1006+127insTAGGCCTGG MANE Select	NP_060116.2:n.1006+126_1006+127insTAGGCCTGG