Canonical Allele Identifier: CA1164144099

Gene: TRIT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.39847088_39847093delinsAGAACT , CM000663.2:g.39847088_39847093delinsAGAACT	GRCh38
NC_000001.10:g.40312760_40312765delinsAGAACT , CM000663.1:g.40312760_40312765delinsAGAACT	GRCh37
NC_000001.9:g.40085347_40085352delinsAGAACT	NCBI36
NG_042822.1:g.41419_41424delinsAGTTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316891.10:c.1006+127_1006+132delinsAGTTCT MANE Select	ENSP00000321810.5:n.1006+127_1006+132delinsAGTTCT
ENST00000648678.1:c.1898+127_1898+132delinsAGTTCT	ENSP00000497805.1:n.1898+127_1898+132delinsAGTTCT
ENST00000316891.9:c.1006+127_1006+132delinsAGTTCT	ENSP00000321810.5:n.1006+127_1006+132delinsAGTTCT
ENST00000372818.5:c.928+455_928+460delinsAGTTCT	ENSP00000361905.1:n.928+455_928+460delinsAGTTCT
ENST00000441669.6:c.760+127_760+132delinsAGTTCT	ENSP00000388333.2:n.760+127_760+132delinsAGTTCT
ENST00000462797.5:c.1006+127_1006+132delinsAGTTCT	ENSP00000473773.1:n.1006+127_1006+132delinsAGTTCT
ENST00000465417.5:n.190+127_190+132delinsAGTTCT
ENST00000467774.1:n.415_420delinsAGTTCT
ENST00000491865.5:n.241+127_241+132delinsAGTTCT
ENST00000492612.6:c.850+127_850+132delinsAGTTCT
ENST00000495175.6:c.*428+127_*428+132delinsAGTTCT	ENSP00000474264.1:n.*428+127_*428+132delinsAGTTCT
ENST00000537440.5:c.94+127_94+132delinsAGTTCT	ENSP00000437700.1:n.94+127_94+132delinsAGTTCT
ENST00000541099.5:c.-140-2453_-140-2448delinsAGTTCT	ENSP00000437896.1:n.-140-2453_-140-2448delinsAGTTCT
NM_001312691.1:c.928+455_928+460delinsAGTTCT	NP_001299620.1:n.928+455_928+460delinsAGTTCT
NM_001312692.1:c.760+127_760+132delinsAGTTCT	NP_001299621.1:n.760+127_760+132delinsAGTTCT
NM_017646.4:c.1006+127_1006+132delinsAGTTCT	NP_060116.2:n.1006+127_1006+132delinsAGTTCT
NM_017646.5:c.1006+127_1006+132delinsAGTTCT	NP_060116.2:n.1006+127_1006+132delinsAGTTCT
NR_132401.1:n.1022+127_1022+132delinsAGTTCT
NR_132402.1:n.880+127_880+132delinsAGTTCT
NR_132403.1:n.876+127_876+132delinsAGTTCT
NR_132404.1:n.876+127_876+132delinsAGTTCT
NR_132405.1:n.872+127_872+132delinsAGTTCT
NR_132406.1:n.763+127_763+132delinsAGTTCT
NR_132407.1:n.640+127_640+132delinsAGTTCT
NR_132408.1:n.636+127_636+132delinsAGTTCT
NR_132409.1:n.497+127_497+132delinsAGTTCT
NR_132410.1:n.523+127_523+132delinsAGTTCT
NR_132412.1:n.384+127_384+132delinsAGTTCT
NR_132413.1:n.195-2453_195-2448delinsAGTTCT
NR_132414.1:n.195-5180_195-5175delinsAGTTCT
NR_132415.1:n.1113+127_1113+132delinsAGTTCT
XM_005270954.1:c.763+127_763+132delinsAGTTCT	XP_005271011.1:n.763+127_763+132delinsAGTTCT
XM_006710706.1:c.583+127_583+132delinsAGTTCT	XP_006710769.1:n.583+127_583+132delinsAGTTCT
XM_005270954.2:c.763+127_763+132delinsAGTTCT	XP_005271011.1:n.763+127_763+132delinsAGTTCT
XR_946672.2:n.1106+127_1106+132delinsAGTTCT
NM_017646.6:c.1006+127_1006+132delinsAGTTCT MANE Select	NP_060116.2:n.1006+127_1006+132delinsAGTTCT