Canonical Allele Identifier: CA1164144089
Gene: TRIT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.39847077_39847078delinsAT , CM000663.2:g.39847077_39847078delinsAT GRCh38
NC_000001.10:g.40312749_40312750delinsAT , CM000663.1:g.40312749_40312750delinsAT GRCh37
NC_000001.9:g.40085336_40085337delinsAT NCBI36
NG_042822.1:g.41434_41435delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000316891.10:c.1006+142_1006+143delinsAT MANE Select ENSP00000321810.5:n.1006+142_1006+143delinsAT
ENST00000648678.1:c.1898+142_1898+143delinsAT ENSP00000497805.1:n.1898+142_1898+143delinsAT
ENST00000316891.9:c.1006+142_1006+143delinsAT ENSP00000321810.5:n.1006+142_1006+143delinsAT
ENST00000372818.5:c.928+470_928+471delinsAT ENSP00000361905.1:n.928+470_928+471delinsAT
ENST00000441669.6:c.760+142_760+143delinsAT ENSP00000388333.2:n.760+142_760+143delinsAT
ENST00000462797.5:c.1006+142_1006+143delinsAT ENSP00000473773.1:n.1006+142_1006+143delinsAT
ENST00000465417.5:n.190+142_190+143delinsAT
ENST00000467774.1:n.430_431delinsAT
ENST00000491865.5:n.241+142_241+143delinsAT
ENST00000492612.6:c.850+142_850+143delinsAT
ENST00000495175.6:c.*428+142_*428+143delinsAT ENSP00000474264.1:n.*428+142_*428+143delinsAT
ENST00000537440.5:c.94+142_94+143delinsAT ENSP00000437700.1:n.94+142_94+143delinsAT
ENST00000541099.5:c.-140-2438_-140-2437delinsAT ENSP00000437896.1:n.-140-2438_-140-2437delinsAT
NM_001312691.1:c.928+470_928+471delinsAT NP_001299620.1:n.928+470_928+471delinsAT
NM_001312692.1:c.760+142_760+143delinsAT NP_001299621.1:n.760+142_760+143delinsAT
NM_017646.4:c.1006+142_1006+143delinsAT NP_060116.2:n.1006+142_1006+143delinsAT
NM_017646.5:c.1006+142_1006+143delinsAT NP_060116.2:n.1006+142_1006+143delinsAT
NR_132401.1:n.1022+142_1022+143delinsAT
NR_132402.1:n.880+142_880+143delinsAT
NR_132403.1:n.876+142_876+143delinsAT
NR_132404.1:n.876+142_876+143delinsAT
NR_132405.1:n.872+142_872+143delinsAT
NR_132406.1:n.763+142_763+143delinsAT
NR_132407.1:n.640+142_640+143delinsAT
NR_132408.1:n.636+142_636+143delinsAT
NR_132409.1:n.497+142_497+143delinsAT
NR_132410.1:n.523+142_523+143delinsAT
NR_132412.1:n.384+142_384+143delinsAT
NR_132413.1:n.195-2438_195-2437delinsAT
NR_132414.1:n.195-5165_195-5164delinsAT
NR_132415.1:n.1113+142_1113+143delinsAT
XM_005270954.1:c.763+142_763+143delinsAT XP_005271011.1:n.763+142_763+143delinsAT
XM_006710706.1:c.583+142_583+143delinsAT XP_006710769.1:n.583+142_583+143delinsAT
XM_005270954.2:c.763+142_763+143delinsAT XP_005271011.1:n.763+142_763+143delinsAT
XR_946672.2:n.1106+142_1106+143delinsAT
NM_017646.6:c.1006+142_1006+143delinsAT MANE Select NP_060116.2:n.1006+142_1006+143delinsAT