Canonical Allele Identifier: CA1164144478
Gene: TRIT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.39847567A= , CM000663.2:g.39847567A= GRCh38
NC_000001.10:g.40313239A= , CM000663.1:g.40313239A= GRCh37
NC_000001.9:g.40085826A= NCBI36
NG_042822.1:g.40945T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000316891.10:c.909T= MANE Select ENSP00000321810.5:p.Ser303=
ENST00000648678.1:c.1801T= ENSP00000497805.1:n.1801T=
ENST00000316891.9:c.909T= ENSP00000321810.5:p.Ser303=
ENST00000372818.5:c.909T= ENSP00000361905.1:p.Ser303=
ENST00000441669.6:c.663T= ENSP00000388333.2:p.Ser221=
ENST00000462797.5:c.909T= ENSP00000473773.1:p.Ser303=
ENST00000465417.5:n.113-270T=
ENST00000467774.1:n.191T=
ENST00000486825.6:c.814T=
ENST00000489945.5:c.*327T= ENSP00000473745.1:n.*327T=
ENST00000491865.5:n.164-270T=
ENST00000492612.6:c.753T=
ENST00000495175.6:c.*331T= ENSP00000474264.1:n.*331T=
ENST00000537440.5:c.17-270T= ENSP00000437700.1:n.17-270T=
ENST00000541099.5:c.-140-2927T= ENSP00000437896.1:n.-140-2927T=
NM_001312691.1:c.909T= NP_001299620.1:p.Ser303=
NM_001312692.1:c.663T= NP_001299621.1:p.Ser221=
NM_017646.4:c.909T= NP_060116.2:p.Ser303=
NM_017646.5:c.909T= NP_060116.2:p.Ser303=
NR_132401.1:n.925T=
NR_132402.1:n.783T=
NR_132403.1:n.779T=
NR_132404.1:n.779T=
NR_132405.1:n.775T=
NR_132406.1:n.686-270T=
NR_132407.1:n.543T=
NR_132408.1:n.539T=
NR_132409.1:n.400T=
NR_132410.1:n.446-270T=
NR_132412.1:n.307-270T=
NR_132413.1:n.195-2927T=
NR_132414.1:n.195-5654T=
NR_132415.1:n.1016T=
XM_005270954.1:c.666T= XP_005271011.1:p.Ser222=
XM_006710706.1:c.486T= XP_006710769.1:p.Ser162=
XM_005270954.2:c.666T= XP_005271011.1:p.Ser222=
XR_946672.2:n.1009T=
NM_017646.6:c.909T= MANE Select NP_060116.2:p.Ser303=