Canonical Allele Identifier: CA1000849891

Gene: TRIT1

Linked Data

• gnomAD v3: 1-39847050-A-ATTTTTT
• gnomAD v4: 1-39847050-A-ATTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.39847051_39847052insTTTTTT , CM000663.2:g.39847051_39847052insTTTTTT	GRCh38
NC_000001.10:g.40312723_40312724insTTTTTT , CM000663.1:g.40312723_40312724insTTTTTT	GRCh37
NC_000001.9:g.40085310_40085311insTTTTTT	NCBI36
NG_042822.1:g.41461_41462insAAAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316891.10:c.1006+169_1006+170insAAAAAA MANE Select	ENSP00000321810.5:n.1006+169_1006+170insAAAAAA
ENST00000648678.1:c.1898+169_1898+170insAAAAAA	ENSP00000497805.1:n.1898+169_1898+170insAAAAAA
ENST00000316891.9:c.1006+169_1006+170insAAAAAA	ENSP00000321810.5:n.1006+169_1006+170insAAAAAA
ENST00000372818.5:c.928+497_928+498insAAAAAA	ENSP00000361905.1:n.928+497_928+498insAAAAAA
ENST00000441669.6:c.760+169_760+170insAAAAAA	ENSP00000388333.2:n.760+169_760+170insAAAAAA
ENST00000462797.5:c.1006+169_1006+170insAAAAAA	ENSP00000473773.1:n.1006+169_1006+170insAAAAAA
ENST00000465417.5:n.190+169_190+170insAAAAAA
ENST00000467774.1:n.457_458insAAAAAA
ENST00000491865.5:n.241+169_241+170insAAAAAA
ENST00000492612.6:c.850+169_850+170insAAAAAA
ENST00000495175.6:c.*428+169_*428+170insAAAAAA	ENSP00000474264.1:n.*428+169_*428+170insAAAAAA
ENST00000537440.5:c.94+169_94+170insAAAAAA	ENSP00000437700.1:n.94+169_94+170insAAAAAA
ENST00000541099.5:c.-140-2411_-140-2410insAAAAAA	ENSP00000437896.1:n.-140-2411_-140-2410insAAAAAA
NM_001312691.1:c.928+497_928+498insAAAAAA	NP_001299620.1:n.928+497_928+498insAAAAAA
NM_001312692.1:c.760+169_760+170insAAAAAA	NP_001299621.1:n.760+169_760+170insAAAAAA
NM_017646.4:c.1006+169_1006+170insAAAAAA	NP_060116.2:n.1006+169_1006+170insAAAAAA
NM_017646.5:c.1006+169_1006+170insAAAAAA	NP_060116.2:n.1006+169_1006+170insAAAAAA
NR_132401.1:n.1022+169_1022+170insAAAAAA
NR_132402.1:n.880+169_880+170insAAAAAA
NR_132403.1:n.876+169_876+170insAAAAAA
NR_132404.1:n.876+169_876+170insAAAAAA
NR_132405.1:n.872+169_872+170insAAAAAA
NR_132406.1:n.763+169_763+170insAAAAAA
NR_132407.1:n.640+169_640+170insAAAAAA
NR_132408.1:n.636+169_636+170insAAAAAA
NR_132409.1:n.497+169_497+170insAAAAAA
NR_132410.1:n.523+169_523+170insAAAAAA
NR_132412.1:n.384+169_384+170insAAAAAA
NR_132413.1:n.195-2411_195-2410insAAAAAA
NR_132414.1:n.195-5138_195-5137insAAAAAA
NR_132415.1:n.1113+169_1113+170insAAAAAA
XM_005270954.1:c.763+169_763+170insAAAAAA	XP_005271011.1:n.763+169_763+170insAAAAAA
XM_006710706.1:c.583+169_583+170insAAAAAA	XP_006710769.1:n.583+169_583+170insAAAAAA
XM_005270954.2:c.763+169_763+170insAAAAAA	XP_005271011.1:n.763+169_763+170insAAAAAA
XR_946672.2:n.1106+169_1106+170insAAAAAA
NM_017646.6:c.1006+169_1006+170insAAAAAA MANE Select	NP_060116.2:n.1006+169_1006+170insAAAAAA