Canonical Allele Identifier: CA1164144255
Gene: TRIT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.39847258C= , CM000663.2:g.39847258C= GRCh38
NC_000001.10:g.40312930C= , CM000663.1:g.40312930C= GRCh37
NC_000001.9:g.40085517C= NCBI36
NG_042822.1:g.41254G=

Transcript Alleles

HGVS Amino-acid Change
NM_017646.6:c.968G= MANE Select NP_060116.2:p.Arg323=
ENST00000316891.10:c.968G= MANE Select ENSP00000321810.5:p.Arg323=
NM_001312691.1:c.928+290G= NP_001299620.1:n.928+290G=
NM_001312692.1:c.722G= NP_001299621.1:p.Arg241=
NM_017646.4:c.968G= NP_060116.2:p.Arg323=
NM_017646.5:c.968G= NP_060116.2:p.Arg323=
NR_132401.1:n.984G=
NR_132402.1:n.842G=
NR_132403.1:n.838G=
NR_132404.1:n.838G=
NR_132405.1:n.834G=
NR_132406.1:n.725G=
NR_132407.1:n.602G=
NR_132408.1:n.598G=
NR_132409.1:n.459G=
NR_132410.1:n.485G=
NR_132412.1:n.346G=
NR_132413.1:n.195-2618G=
NR_132414.1:n.195-5345G=
NR_132415.1:n.1075G=
ENST00000316891.9:c.968G= ENSP00000321810.5:p.Arg323=
ENST00000372818.5:c.928+290G= ENSP00000361905.1:n.928+290G=
ENST00000441669.6:c.722G= ENSP00000388333.2:p.Arg241=
ENST00000462797.5:c.968G= ENSP00000473773.1:p.Arg323=
ENST00000465417.5:n.152G=
ENST00000467774.1:n.250G=
ENST00000489945.5:c.*386G= ENSP00000473745.1:n.*386G=
ENST00000491865.5:n.203G=
ENST00000492612.6:c.812G=
ENST00000495175.6:c.*390G= ENSP00000474264.1:n.*390G=
ENST00000537440.5:c.56G= ENSP00000437700.1:p.Arg19=
ENST00000541099.5:c.-140-2618G= ENSP00000437896.1:n.-140-2618G=
ENST00000648678.1:c.1860G= ENSP00000497805.1:n.1860G=
XM_005270954.1:c.725G= XP_005271011.1:p.Arg242=
XM_005270954.2:c.725G= XP_005271011.1:p.Arg242=
XM_006710706.1:c.545G= XP_006710769.1:p.Arg182=
XR_946672.2:n.1068G=