Canonical Allele Identifier: CA1164144477
Gene: TRIT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.39847566T= , CM000663.2:g.39847566T= GRCh38
NC_000001.10:g.40313238T= , CM000663.1:g.40313238T= GRCh37
NC_000001.9:g.40085825T= NCBI36
NG_042822.1:g.40946A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000316891.10:c.910A= MANE Select ENSP00000321810.5:p.Asn304=
ENST00000648678.1:c.1802A= ENSP00000497805.1:n.1802A=
ENST00000316891.9:c.910A= ENSP00000321810.5:p.Asn304=
ENST00000372818.5:c.910A= ENSP00000361905.1:p.Asn304=
ENST00000441669.6:c.664A= ENSP00000388333.2:p.Asn222=
ENST00000462797.5:c.910A= ENSP00000473773.1:p.Asn304=
ENST00000465417.5:n.113-269A=
ENST00000467774.1:n.192A=
ENST00000486825.6:c.815A=
ENST00000489945.5:c.*328A= ENSP00000473745.1:n.*328A=
ENST00000491865.5:n.164-269A=
ENST00000492612.6:c.754A=
ENST00000495175.6:c.*332A= ENSP00000474264.1:n.*332A=
ENST00000537440.5:c.17-269A= ENSP00000437700.1:n.17-269A=
ENST00000541099.5:c.-140-2926A= ENSP00000437896.1:n.-140-2926A=
NM_001312691.1:c.910A= NP_001299620.1:p.Asn304=
NM_001312692.1:c.664A= NP_001299621.1:p.Asn222=
NM_017646.4:c.910A= NP_060116.2:p.Asn304=
NM_017646.5:c.910A= NP_060116.2:p.Asn304=
NR_132401.1:n.926A=
NR_132402.1:n.784A=
NR_132403.1:n.780A=
NR_132404.1:n.780A=
NR_132405.1:n.776A=
NR_132406.1:n.686-269A=
NR_132407.1:n.544A=
NR_132408.1:n.540A=
NR_132409.1:n.401A=
NR_132410.1:n.446-269A=
NR_132412.1:n.307-269A=
NR_132413.1:n.195-2926A=
NR_132414.1:n.195-5653A=
NR_132415.1:n.1017A=
XM_005270954.1:c.667A= XP_005271011.1:p.Asn223=
XM_006710706.1:c.487A= XP_006710769.1:p.Asn163=
XM_005270954.2:c.667A= XP_005271011.1:p.Asn223=
XR_946672.2:n.1010A=
NM_017646.6:c.910A= MANE Select NP_060116.2:p.Asn304=