Canonical Allele Identifier: CA1164144472
Gene: TRIT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.39847549T= , CM000663.2:g.39847549T= GRCh38
NC_000001.10:g.40313221T= , CM000663.1:g.40313221T= GRCh37
NC_000001.9:g.40085808T= NCBI36
NG_042822.1:g.40963A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000316891.10:c.927A= MANE Select ENSP00000321810.5:p.Lys309=
ENST00000648678.1:c.1819A= ENSP00000497805.1:n.1819A=
ENST00000316891.9:c.927A= ENSP00000321810.5:p.Lys309=
ENST00000372818.5:c.927A= ENSP00000361905.1:p.Lys309=
ENST00000441669.6:c.681A= ENSP00000388333.2:p.Lys227=
ENST00000462797.5:c.927A= ENSP00000473773.1:p.Lys309=
ENST00000465417.5:n.113-252A=
ENST00000467774.1:n.209A=
ENST00000486825.6:c.832A=
ENST00000489945.5:c.*345A= ENSP00000473745.1:n.*345A=
ENST00000491865.5:n.164-252A=
ENST00000492612.6:c.771A=
ENST00000495175.6:c.*349A= ENSP00000474264.1:n.*349A=
ENST00000537440.5:c.17-252A= ENSP00000437700.1:n.17-252A=
ENST00000541099.5:c.-140-2909A= ENSP00000437896.1:n.-140-2909A=
NM_001312691.1:c.927A= NP_001299620.1:p.Lys309=
NM_001312692.1:c.681A= NP_001299621.1:p.Lys227=
NM_017646.4:c.927A= NP_060116.2:p.Lys309=
NM_017646.5:c.927A= NP_060116.2:p.Lys309=
NR_132401.1:n.943A=
NR_132402.1:n.801A=
NR_132403.1:n.797A=
NR_132404.1:n.797A=
NR_132405.1:n.793A=
NR_132406.1:n.686-252A=
NR_132407.1:n.561A=
NR_132408.1:n.557A=
NR_132409.1:n.418A=
NR_132410.1:n.446-252A=
NR_132412.1:n.307-252A=
NR_132413.1:n.195-2909A=
NR_132414.1:n.195-5636A=
NR_132415.1:n.1034A=
XM_005270954.1:c.684A= XP_005271011.1:p.Lys228=
XM_006710706.1:c.504A= XP_006710769.1:p.Lys168=
XM_005270954.2:c.684A= XP_005271011.1:p.Lys228=
XR_946672.2:n.1027A=
NM_017646.6:c.927A= MANE Select NP_060116.2:p.Lys309=