Canonical Allele Identifier: CA339832668

Gene: TRIT1

Linked Data

• MyVariant Identifiers: chr1:g.40312922T>A (hg19) ; chr1:g.39847250T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.39847250T>A , CM000663.2:g.39847250T>A	GRCh38
NC_000001.10:g.40312922T>A , CM000663.1:g.40312922T>A	GRCh37
NC_000001.9:g.40085509T>A	NCBI36
NG_042822.1:g.41262A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316891.10:c.976A>T MANE Select	ENSP00000321810.5:p.Asn326Tyr
ENST00000648678.1:c.1868A>T	ENSP00000497805.1:n.1868A>T
ENST00000316891.9:c.976A>T	ENSP00000321810.5:p.Asn326Tyr
ENST00000372818.5:c.928+298A>T	ENSP00000361905.1:n.928+298A>T
ENST00000441669.6:c.730A>T	ENSP00000388333.2:p.Asn244Tyr
ENST00000462797.5:c.976A>T	ENSP00000473773.1:p.Asn326Tyr
ENST00000465417.5:n.160A>T
ENST00000467774.1:n.258A>T
ENST00000489945.5:c.*394A>T	ENSP00000473745.1:n.*394A>T
ENST00000491865.5:n.211A>T
ENST00000492612.6:c.820A>T
ENST00000495175.6:c.*398A>T	ENSP00000474264.1:n.*398A>T
ENST00000537440.5:c.64A>T	ENSP00000437700.1:p.Asn22Tyr
ENST00000541099.5:c.-140-2610A>T	ENSP00000437896.1:n.-140-2610A>T
NM_001312691.1:c.928+298A>T	NP_001299620.1:n.928+298A>T
NM_001312692.1:c.730A>T	NP_001299621.1:p.Asn244Tyr
NM_017646.4:c.976A>T	NP_060116.2:p.Asn326Tyr
NM_017646.5:c.976A>T	NP_060116.2:p.Asn326Tyr
NR_132401.1:n.992A>T
NR_132402.1:n.850A>T
NR_132403.1:n.846A>T
NR_132404.1:n.846A>T
NR_132405.1:n.842A>T
NR_132406.1:n.733A>T
NR_132407.1:n.610A>T
NR_132408.1:n.606A>T
NR_132409.1:n.467A>T
NR_132410.1:n.493A>T
NR_132412.1:n.354A>T
NR_132413.1:n.195-2610A>T
NR_132414.1:n.195-5337A>T
NR_132415.1:n.1083A>T
XM_005270954.1:c.733A>T	XP_005271011.1:p.Asn245Tyr
XM_006710706.1:c.553A>T	XP_006710769.1:p.Asn185Tyr
XM_005270954.2:c.733A>T	XP_005271011.1:p.Asn245Tyr
XR_946672.2:n.1076A>T
NM_017646.6:c.976A>T MANE Select	NP_060116.2:p.Asn326Tyr