Canonical Allele Identifier: CA339833231

Gene: TRIT1

Linked Data

• MyVariant Identifiers: chr1:g.40313234T>G (hg19) ; chr1:g.39847562T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.39847562T>G , CM000663.2:g.39847562T>G	GRCh38
NC_000001.10:g.40313234T>G , CM000663.1:g.40313234T>G	GRCh37
NC_000001.9:g.40085821T>G	NCBI36
NG_042822.1:g.40950A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316891.10:c.914A>C MANE Select	ENSP00000321810.5:p.Gln305Pro
ENST00000648678.1:c.1806A>C	ENSP00000497805.1:n.1806A>C
ENST00000316891.9:c.914A>C	ENSP00000321810.5:p.Gln305Pro
ENST00000372818.5:c.914A>C	ENSP00000361905.1:p.Gln305Pro
ENST00000441669.6:c.668A>C	ENSP00000388333.2:p.Gln223Pro
ENST00000462797.5:c.914A>C	ENSP00000473773.1:p.Gln305Pro
ENST00000465417.5:n.113-265A>C
ENST00000467774.1:n.196A>C
ENST00000486825.6:c.819A>C
ENST00000489945.5:c.*332A>C	ENSP00000473745.1:n.*332A>C
ENST00000491865.5:n.164-265A>C
ENST00000492612.6:c.758A>C
ENST00000495175.6:c.*336A>C	ENSP00000474264.1:n.*336A>C
ENST00000537440.5:c.17-265A>C	ENSP00000437700.1:n.17-265A>C
ENST00000541099.5:c.-140-2922A>C	ENSP00000437896.1:n.-140-2922A>C
NM_001312691.1:c.914A>C	NP_001299620.1:p.Gln305Pro
NM_001312692.1:c.668A>C	NP_001299621.1:p.Gln223Pro
NM_017646.4:c.914A>C	NP_060116.2:p.Gln305Pro
NM_017646.5:c.914A>C	NP_060116.2:p.Gln305Pro
NR_132401.1:n.930A>C
NR_132402.1:n.788A>C
NR_132403.1:n.784A>C
NR_132404.1:n.784A>C
NR_132405.1:n.780A>C
NR_132406.1:n.686-265A>C
NR_132407.1:n.548A>C
NR_132408.1:n.544A>C
NR_132409.1:n.405A>C
NR_132410.1:n.446-265A>C
NR_132412.1:n.307-265A>C
NR_132413.1:n.195-2922A>C
NR_132414.1:n.195-5649A>C
NR_132415.1:n.1021A>C
XM_005270954.1:c.671A>C	XP_005271011.1:p.Gln224Pro
XM_006710706.1:c.491A>C	XP_006710769.1:p.Gln164Pro
XM_005270954.2:c.671A>C	XP_005271011.1:p.Gln224Pro
XR_946672.2:n.1014A>C
NM_017646.6:c.914A>C MANE Select	NP_060116.2:p.Gln305Pro