Canonical Allele Identifier: CA339832896

Gene: TRIT1

Linked Data

• MyVariant Identifiers: chr1:g.40312954T>G (hg19) ; chr1:g.39847282T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.39847282T>G , CM000663.2:g.39847282T>G	GRCh38
NC_000001.10:g.40312954T>G , CM000663.1:g.40312954T>G	GRCh37
NC_000001.9:g.40085541T>G	NCBI36
NG_042822.1:g.41230A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316891.10:c.944A>C MANE Select	ENSP00000321810.5:p.Lys315Thr
ENST00000648678.1:c.1836A>C	ENSP00000497805.1:n.1836A>C
ENST00000316891.9:c.944A>C	ENSP00000321810.5:p.Lys315Thr
ENST00000372818.5:c.928+266A>C	ENSP00000361905.1:n.928+266A>C
ENST00000441669.6:c.698A>C	ENSP00000388333.2:p.Lys233Thr
ENST00000462797.5:c.944A>C	ENSP00000473773.1:p.Lys315Thr
ENST00000465417.5:n.128A>C
ENST00000467774.1:n.226A>C
ENST00000486825.6:c.849A>C
ENST00000489945.5:c.*362A>C	ENSP00000473745.1:n.*362A>C
ENST00000491865.5:n.179A>C
ENST00000492612.6:c.788A>C
ENST00000495175.6:c.*366A>C	ENSP00000474264.1:n.*366A>C
ENST00000537440.5:c.32A>C	ENSP00000437700.1:p.Lys11Thr
ENST00000541099.5:c.-140-2642A>C	ENSP00000437896.1:n.-140-2642A>C
NM_001312691.1:c.928+266A>C	NP_001299620.1:n.928+266A>C
NM_001312692.1:c.698A>C	NP_001299621.1:p.Lys233Thr
NM_017646.4:c.944A>C	NP_060116.2:p.Lys315Thr
NM_017646.5:c.944A>C	NP_060116.2:p.Lys315Thr
NR_132401.1:n.960A>C
NR_132402.1:n.818A>C
NR_132403.1:n.814A>C
NR_132404.1:n.814A>C
NR_132405.1:n.810A>C
NR_132406.1:n.701A>C
NR_132407.1:n.578A>C
NR_132408.1:n.574A>C
NR_132409.1:n.435A>C
NR_132410.1:n.461A>C
NR_132412.1:n.322A>C
NR_132413.1:n.195-2642A>C
NR_132414.1:n.195-5369A>C
NR_132415.1:n.1051A>C
XM_005270954.1:c.701A>C	XP_005271011.1:p.Lys234Thr
XM_006710706.1:c.521A>C	XP_006710769.1:p.Lys174Thr
XM_005270954.2:c.701A>C	XP_005271011.1:p.Lys234Thr
XR_946672.2:n.1044A>C
NM_017646.6:c.944A>C MANE Select	NP_060116.2:p.Lys315Thr