Canonical Allele Identifier: CA2645075236

Gene: TRIT1

Linked Data

• gnomAD v4: 1-39847029-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.39847029_39847030insT , CM000663.2:g.39847029_39847030insT	GRCh38
NC_000001.10:g.40312701_40312702insT , CM000663.1:g.40312701_40312702insT	GRCh37
NC_000001.9:g.40085288_40085289insT	NCBI36
NG_042822.1:g.41482_41483insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316891.10:c.1006+190_1006+191insA MANE Select	ENSP00000321810.5:n.1006+190_1006+191insA
ENST00000648678.1:c.1898+190_1898+191insA	ENSP00000497805.1:n.1898+190_1898+191insA
ENST00000316891.9:c.1006+190_1006+191insA	ENSP00000321810.5:n.1006+190_1006+191insA
ENST00000372818.5:c.928+518_928+519insA	ENSP00000361905.1:n.928+518_928+519insA
ENST00000441669.6:c.760+190_760+191insA	ENSP00000388333.2:n.760+190_760+191insA
ENST00000462797.5:c.1006+190_1006+191insA	ENSP00000473773.1:n.1006+190_1006+191insA
ENST00000465417.5:n.190+190_190+191insA
ENST00000491865.5:n.241+190_241+191insA
ENST00000492612.6:c.850+190_850+191insA
ENST00000495175.6:c.*428+190_*428+191insA	ENSP00000474264.1:n.*428+190_*428+191insA
ENST00000537440.5:c.94+190_94+191insA	ENSP00000437700.1:n.94+190_94+191insA
ENST00000541099.5:c.-140-2390_-140-2389insA	ENSP00000437896.1:n.-140-2390_-140-2389insA
NM_001312691.1:c.928+518_928+519insA	NP_001299620.1:n.928+518_928+519insA
NM_001312692.1:c.760+190_760+191insA	NP_001299621.1:n.760+190_760+191insA
NM_017646.4:c.1006+190_1006+191insA	NP_060116.2:n.1006+190_1006+191insA
NM_017646.5:c.1006+190_1006+191insA	NP_060116.2:n.1006+190_1006+191insA
NR_132401.1:n.1022+190_1022+191insA
NR_132402.1:n.880+190_880+191insA
NR_132403.1:n.876+190_876+191insA
NR_132404.1:n.876+190_876+191insA
NR_132405.1:n.872+190_872+191insA
NR_132406.1:n.763+190_763+191insA
NR_132407.1:n.640+190_640+191insA
NR_132408.1:n.636+190_636+191insA
NR_132409.1:n.497+190_497+191insA
NR_132410.1:n.523+190_523+191insA
NR_132412.1:n.384+190_384+191insA
NR_132413.1:n.195-2390_195-2389insA
NR_132414.1:n.195-5117_195-5116insA
NR_132415.1:n.1113+190_1113+191insA
XM_005270954.1:c.763+190_763+191insA	XP_005271011.1:n.763+190_763+191insA
XM_006710706.1:c.583+190_583+191insA	XP_006710769.1:n.583+190_583+191insA
XM_005270954.2:c.763+190_763+191insA	XP_005271011.1:n.763+190_763+191insA
XR_946672.2:n.1106+190_1106+191insA
NM_017646.6:c.1006+190_1006+191insA MANE Select	NP_060116.2:n.1006+190_1006+191insA