Canonical Allele Identifier: CA339832686

Gene: TRIT1

Linked Data

• MyVariant Identifiers: chr1:g.40312924T>G (hg19) ; chr1:g.39847252T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.39847252T>G , CM000663.2:g.39847252T>G	GRCh38
NC_000001.10:g.40312924T>G , CM000663.1:g.40312924T>G	GRCh37
NC_000001.9:g.40085511T>G	NCBI36
NG_042822.1:g.41260A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316891.10:c.974A>C MANE Select	ENSP00000321810.5:p.Gln325Pro
ENST00000648678.1:c.1866A>C	ENSP00000497805.1:n.1866A>C
ENST00000316891.9:c.974A>C	ENSP00000321810.5:p.Gln325Pro
ENST00000372818.5:c.928+296A>C	ENSP00000361905.1:n.928+296A>C
ENST00000441669.6:c.728A>C	ENSP00000388333.2:p.Gln243Pro
ENST00000462797.5:c.974A>C	ENSP00000473773.1:p.Gln325Pro
ENST00000465417.5:n.158A>C
ENST00000467774.1:n.256A>C
ENST00000489945.5:c.*392A>C	ENSP00000473745.1:n.*392A>C
ENST00000491865.5:n.209A>C
ENST00000492612.6:c.818A>C
ENST00000495175.6:c.*396A>C	ENSP00000474264.1:n.*396A>C
ENST00000537440.5:c.62A>C	ENSP00000437700.1:p.Gln21Pro
ENST00000541099.5:c.-140-2612A>C	ENSP00000437896.1:n.-140-2612A>C
NM_001312691.1:c.928+296A>C	NP_001299620.1:n.928+296A>C
NM_001312692.1:c.728A>C	NP_001299621.1:p.Gln243Pro
NM_017646.4:c.974A>C	NP_060116.2:p.Gln325Pro
NM_017646.5:c.974A>C	NP_060116.2:p.Gln325Pro
NR_132401.1:n.990A>C
NR_132402.1:n.848A>C
NR_132403.1:n.844A>C
NR_132404.1:n.844A>C
NR_132405.1:n.840A>C
NR_132406.1:n.731A>C
NR_132407.1:n.608A>C
NR_132408.1:n.604A>C
NR_132409.1:n.465A>C
NR_132410.1:n.491A>C
NR_132412.1:n.352A>C
NR_132413.1:n.195-2612A>C
NR_132414.1:n.195-5339A>C
NR_132415.1:n.1081A>C
XM_005270954.1:c.731A>C	XP_005271011.1:p.Gln244Pro
XM_006710706.1:c.551A>C	XP_006710769.1:p.Gln184Pro
XM_005270954.2:c.731A>C	XP_005271011.1:p.Gln244Pro
XR_946672.2:n.1074A>C
NM_017646.6:c.974A>C MANE Select	NP_060116.2:p.Gln325Pro