Canonical Allele Identifier: CA735704725

Gene: TRIT1

Linked Data

• dbSNP Id: rs1225566187
• gnomAD v4: 1-39847043-T-TG
• MyVariant Identifiers: chr1:g.40312715_40312716insG (hg19) ; chr1:g.39847043_39847044insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.39847043_39847044insG , CM000663.2:g.39847043_39847044insG	GRCh38
NC_000001.10:g.40312715_40312716insG , CM000663.1:g.40312715_40312716insG	GRCh37
NC_000001.9:g.40085302_40085303insG	NCBI36
NG_042822.1:g.41468_41469insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316891.10:c.1006+176_1006+177insC MANE Select	ENSP00000321810.5:n.1006+176_1006+177insC
ENST00000648678.1:c.1898+176_1898+177insC	ENSP00000497805.1:n.1898+176_1898+177insC
ENST00000316891.9:c.1006+176_1006+177insC	ENSP00000321810.5:n.1006+176_1006+177insC
ENST00000372818.5:c.928+504_928+505insC	ENSP00000361905.1:n.928+504_928+505insC
ENST00000441669.6:c.760+176_760+177insC	ENSP00000388333.2:n.760+176_760+177insC
ENST00000462797.5:c.1006+176_1006+177insC	ENSP00000473773.1:n.1006+176_1006+177insC
ENST00000465417.5:n.190+176_190+177insC
ENST00000491865.5:n.241+176_241+177insC
ENST00000492612.6:c.850+176_850+177insC
ENST00000495175.6:c.*428+176_*428+177insC	ENSP00000474264.1:n.*428+176_*428+177insC
ENST00000537440.5:c.94+176_94+177insC	ENSP00000437700.1:n.94+176_94+177insC
ENST00000541099.5:c.-140-2404_-140-2403insC	ENSP00000437896.1:n.-140-2404_-140-2403insC
NM_001312691.1:c.928+504_928+505insC	NP_001299620.1:n.928+504_928+505insC
NM_001312692.1:c.760+176_760+177insC	NP_001299621.1:n.760+176_760+177insC
NM_017646.4:c.1006+176_1006+177insC	NP_060116.2:n.1006+176_1006+177insC
NM_017646.5:c.1006+176_1006+177insC	NP_060116.2:n.1006+176_1006+177insC
NR_132401.1:n.1022+176_1022+177insC
NR_132402.1:n.880+176_880+177insC
NR_132403.1:n.876+176_876+177insC
NR_132404.1:n.876+176_876+177insC
NR_132405.1:n.872+176_872+177insC
NR_132406.1:n.763+176_763+177insC
NR_132407.1:n.640+176_640+177insC
NR_132408.1:n.636+176_636+177insC
NR_132409.1:n.497+176_497+177insC
NR_132410.1:n.523+176_523+177insC
NR_132412.1:n.384+176_384+177insC
NR_132413.1:n.195-2404_195-2403insC
NR_132414.1:n.195-5131_195-5130insC
NR_132415.1:n.1113+176_1113+177insC
XM_005270954.1:c.763+176_763+177insC	XP_005271011.1:n.763+176_763+177insC
XM_006710706.1:c.583+176_583+177insC	XP_006710769.1:n.583+176_583+177insC
XM_005270954.2:c.763+176_763+177insC	XP_005271011.1:n.763+176_763+177insC
XR_946672.2:n.1106+176_1106+177insC
NM_017646.6:c.1006+176_1006+177insC MANE Select	NP_060116.2:n.1006+176_1006+177insC