Canonical Allele Identifier: CA339833242
Gene: TRIT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.39847563G>T , CM000663.2:g.39847563G>T GRCh38
NC_000001.10:g.40313235G>T , CM000663.1:g.40313235G>T GRCh37
NC_000001.9:g.40085822G>T NCBI36
NG_042822.1:g.40949C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000316891.10:c.913C>A MANE Select ENSP00000321810.5:p.Gln305Lys
ENST00000648678.1:c.1805C>A ENSP00000497805.1:n.1805C>A
ENST00000316891.9:c.913C>A ENSP00000321810.5:p.Gln305Lys
ENST00000372818.5:c.913C>A ENSP00000361905.1:p.Gln305Lys
ENST00000441669.6:c.667C>A ENSP00000388333.2:p.Gln223Lys
ENST00000462797.5:c.913C>A ENSP00000473773.1:p.Gln305Lys
ENST00000465417.5:n.113-266C>A
ENST00000467774.1:n.195C>A
ENST00000486825.6:c.818C>A
ENST00000489945.5:c.*331C>A ENSP00000473745.1:n.*331C>A
ENST00000491865.5:n.164-266C>A
ENST00000492612.6:c.757C>A
ENST00000495175.6:c.*335C>A ENSP00000474264.1:n.*335C>A
ENST00000537440.5:c.17-266C>A ENSP00000437700.1:n.17-266C>A
ENST00000541099.5:c.-140-2923C>A ENSP00000437896.1:n.-140-2923C>A
NM_001312691.1:c.913C>A NP_001299620.1:p.Gln305Lys
NM_001312692.1:c.667C>A NP_001299621.1:p.Gln223Lys
NM_017646.4:c.913C>A NP_060116.2:p.Gln305Lys
NM_017646.5:c.913C>A NP_060116.2:p.Gln305Lys
NR_132401.1:n.929C>A
NR_132402.1:n.787C>A
NR_132403.1:n.783C>A
NR_132404.1:n.783C>A
NR_132405.1:n.779C>A
NR_132406.1:n.686-266C>A
NR_132407.1:n.547C>A
NR_132408.1:n.543C>A
NR_132409.1:n.404C>A
NR_132410.1:n.446-266C>A
NR_132412.1:n.307-266C>A
NR_132413.1:n.195-2923C>A
NR_132414.1:n.195-5650C>A
NR_132415.1:n.1020C>A
XM_005270954.1:c.670C>A XP_005271011.1:p.Gln224Lys
XM_006710706.1:c.490C>A XP_006710769.1:p.Gln164Lys
XM_005270954.2:c.670C>A XP_005271011.1:p.Gln224Lys
XR_946672.2:n.1013C>A
NM_017646.6:c.913C>A MANE Select NP_060116.2:p.Gln305Lys