Canonical Allele Identifier: CA2510743974

Gene: TRIT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.39847004_39847005insCTAAATTTGGT , CM000663.2:g.39847004_39847005insCTAAATTTGGT	GRCh38
NC_000001.10:g.40312676_40312677insCTAAATTTGGT , CM000663.1:g.40312676_40312677insCTAAATTTGGT	GRCh37
NC_000001.9:g.40085263_40085264insCTAAATTTGGT	NCBI36
NG_042822.1:g.41507_41508insACCAAATTTAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316891.10:c.1006+215_1006+216insACCAAATTTAG MANE Select	ENSP00000321810.5:n.1006+215_1006+216insACCAAATTTAG
ENST00000648678.1:c.1898+215_1898+216insACCAAATTTAG	ENSP00000497805.1:n.1898+215_1898+216insACCAAATTTAG
ENST00000316891.9:c.1006+215_1006+216insACCAAATTTAG	ENSP00000321810.5:n.1006+215_1006+216insACCAAATTTAG
ENST00000372818.5:c.928+543_928+544insACCAAATTTAG	ENSP00000361905.1:n.928+543_928+544insACCAAATTTAG
ENST00000441669.6:c.760+215_760+216insACCAAATTTAG	ENSP00000388333.2:n.760+215_760+216insACCAAATTTAG
ENST00000462797.5:c.1006+215_1006+216insACCAAATTTAG	ENSP00000473773.1:n.1006+215_1006+216insACCAAATTTAG
ENST00000465417.5:n.190+215_190+216insACCAAATTTAG
ENST00000491865.5:n.241+215_241+216insACCAAATTTAG
ENST00000492612.6:c.850+215_850+216insACCAAATTTAG
ENST00000495175.6:c.*428+215_*428+216insACCAAATTTAG	ENSP00000474264.1:n.*428+215_*428+216insACCAAATTTAG
ENST00000537440.5:c.94+215_94+216insACCAAATTTAG	ENSP00000437700.1:n.94+215_94+216insACCAAATTTAG
ENST00000541099.5:c.-140-2365_-140-2364insACCAAATTTAG	ENSP00000437896.1:n.-140-2365_-140-2364insACCAAATTTAG
NM_001312691.1:c.928+543_928+544insACCAAATTTAG	NP_001299620.1:n.928+543_928+544insACCAAATTTAG
NM_001312692.1:c.760+215_760+216insACCAAATTTAG	NP_001299621.1:n.760+215_760+216insACCAAATTTAG
NM_017646.4:c.1006+215_1006+216insACCAAATTTAG	NP_060116.2:n.1006+215_1006+216insACCAAATTTAG
NM_017646.5:c.1006+215_1006+216insACCAAATTTAG	NP_060116.2:n.1006+215_1006+216insACCAAATTTAG
NR_132401.1:n.1022+215_1022+216insACCAAATTTAG
NR_132402.1:n.880+215_880+216insACCAAATTTAG
NR_132403.1:n.876+215_876+216insACCAAATTTAG
NR_132404.1:n.876+215_876+216insACCAAATTTAG
NR_132405.1:n.872+215_872+216insACCAAATTTAG
NR_132406.1:n.763+215_763+216insACCAAATTTAG
NR_132407.1:n.640+215_640+216insACCAAATTTAG
NR_132408.1:n.636+215_636+216insACCAAATTTAG
NR_132409.1:n.497+215_497+216insACCAAATTTAG
NR_132410.1:n.523+215_523+216insACCAAATTTAG
NR_132412.1:n.384+215_384+216insACCAAATTTAG
NR_132413.1:n.195-2365_195-2364insACCAAATTTAG
NR_132414.1:n.195-5092_195-5091insACCAAATTTAG
NR_132415.1:n.1113+215_1113+216insACCAAATTTAG
XM_005270954.1:c.763+215_763+216insACCAAATTTAG	XP_005271011.1:n.763+215_763+216insACCAAATTTAG
XM_006710706.1:c.583+215_583+216insACCAAATTTAG	XP_006710769.1:n.583+215_583+216insACCAAATTTAG
XM_005270954.2:c.763+215_763+216insACCAAATTTAG	XP_005271011.1:n.763+215_763+216insACCAAATTTAG
XR_946672.2:n.1106+215_1106+216insACCAAATTTAG
NM_017646.6:c.1006+215_1006+216insACCAAATTTAG MANE Select	NP_060116.2:n.1006+215_1006+216insACCAAATTTAG