Canonical Allele Identifier: CA1164144044

Gene: TRIT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.39847029_39847034delinsAATTTT , CM000663.2:g.39847029_39847034delinsAATTTT	GRCh38
NC_000001.10:g.40312701_40312706delinsAATTTT , CM000663.1:g.40312701_40312706delinsAATTTT	GRCh37
NC_000001.9:g.40085288_40085293delinsAATTTT	NCBI36
NG_042822.1:g.41478_41483delinsAAAATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316891.10:c.1006+186_1006+191delinsAAAATT MANE Select	ENSP00000321810.5:n.1006+186_1006+191delinsAAAATT
ENST00000648678.1:c.1898+186_1898+191delinsAAAATT	ENSP00000497805.1:n.1898+186_1898+191delinsAAAATT
ENST00000316891.9:c.1006+186_1006+191delinsAAAATT	ENSP00000321810.5:n.1006+186_1006+191delinsAAAATT
ENST00000372818.5:c.928+514_928+519delinsAAAATT	ENSP00000361905.1:n.928+514_928+519delinsAAAATT
ENST00000441669.6:c.760+186_760+191delinsAAAATT	ENSP00000388333.2:n.760+186_760+191delinsAAAATT
ENST00000462797.5:c.1006+186_1006+191delinsAAAATT	ENSP00000473773.1:n.1006+186_1006+191delinsAAAATT
ENST00000465417.5:n.190+186_190+191delinsAAAATT
ENST00000491865.5:n.241+186_241+191delinsAAAATT
ENST00000492612.6:c.850+186_850+191delinsAAAATT
ENST00000495175.6:c.*428+186_*428+191delinsAAAATT	ENSP00000474264.1:n.*428+186_*428+191delinsAAAATT
ENST00000537440.5:c.94+186_94+191delinsAAAATT	ENSP00000437700.1:n.94+186_94+191delinsAAAATT
ENST00000541099.5:c.-140-2394_-140-2389delinsAAAATT	ENSP00000437896.1:n.-140-2394_-140-2389delinsAAAATT
NM_001312691.1:c.928+514_928+519delinsAAAATT	NP_001299620.1:n.928+514_928+519delinsAAAATT
NM_001312692.1:c.760+186_760+191delinsAAAATT	NP_001299621.1:n.760+186_760+191delinsAAAATT
NM_017646.4:c.1006+186_1006+191delinsAAAATT	NP_060116.2:n.1006+186_1006+191delinsAAAATT
NM_017646.5:c.1006+186_1006+191delinsAAAATT	NP_060116.2:n.1006+186_1006+191delinsAAAATT
NR_132401.1:n.1022+186_1022+191delinsAAAATT
NR_132402.1:n.880+186_880+191delinsAAAATT
NR_132403.1:n.876+186_876+191delinsAAAATT
NR_132404.1:n.876+186_876+191delinsAAAATT
NR_132405.1:n.872+186_872+191delinsAAAATT
NR_132406.1:n.763+186_763+191delinsAAAATT
NR_132407.1:n.640+186_640+191delinsAAAATT
NR_132408.1:n.636+186_636+191delinsAAAATT
NR_132409.1:n.497+186_497+191delinsAAAATT
NR_132410.1:n.523+186_523+191delinsAAAATT
NR_132412.1:n.384+186_384+191delinsAAAATT
NR_132413.1:n.195-2394_195-2389delinsAAAATT
NR_132414.1:n.195-5121_195-5116delinsAAAATT
NR_132415.1:n.1113+186_1113+191delinsAAAATT
XM_005270954.1:c.763+186_763+191delinsAAAATT	XP_005271011.1:n.763+186_763+191delinsAAAATT
XM_006710706.1:c.583+186_583+191delinsAAAATT	XP_006710769.1:n.583+186_583+191delinsAAAATT
XM_005270954.2:c.763+186_763+191delinsAAAATT	XP_005271011.1:n.763+186_763+191delinsAAAATT
XR_946672.2:n.1106+186_1106+191delinsAAAATT
NM_017646.6:c.1006+186_1006+191delinsAAAATT MANE Select	NP_060116.2:n.1006+186_1006+191delinsAAAATT