Canonical Allele Identifier: CA339833283

Gene: TRIT1

Linked Data

• MyVariant Identifiers: chr1:g.40313241T>G (hg19) ; chr1:g.39847569T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.39847569T>G , CM000663.2:g.39847569T>G	GRCh38
NC_000001.10:g.40313241T>G , CM000663.1:g.40313241T>G	GRCh37
NC_000001.9:g.40085828T>G	NCBI36
NG_042822.1:g.40943A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316891.10:c.907A>C MANE Select	ENSP00000321810.5:p.Ser303Arg
ENST00000648678.1:c.1799A>C	ENSP00000497805.1:n.1799A>C
ENST00000316891.9:c.907A>C	ENSP00000321810.5:p.Ser303Arg
ENST00000372818.5:c.907A>C	ENSP00000361905.1:p.Ser303Arg
ENST00000441669.6:c.661A>C	ENSP00000388333.2:p.Ser221Arg
ENST00000462797.5:c.907A>C	ENSP00000473773.1:p.Ser303Arg
ENST00000465417.5:n.113-272A>C
ENST00000467774.1:n.189A>C
ENST00000486825.6:c.812A>C
ENST00000489945.5:c.*325A>C	ENSP00000473745.1:n.*325A>C
ENST00000491865.5:n.164-272A>C
ENST00000492612.6:c.751A>C
ENST00000495175.6:c.*329A>C	ENSP00000474264.1:n.*329A>C
ENST00000537440.5:c.17-272A>C	ENSP00000437700.1:n.17-272A>C
ENST00000541099.5:c.-140-2929A>C	ENSP00000437896.1:n.-140-2929A>C
NM_001312691.1:c.907A>C	NP_001299620.1:p.Ser303Arg
NM_001312692.1:c.661A>C	NP_001299621.1:p.Ser221Arg
NM_017646.4:c.907A>C	NP_060116.2:p.Ser303Arg
NM_017646.5:c.907A>C	NP_060116.2:p.Ser303Arg
NR_132401.1:n.923A>C
NR_132402.1:n.781A>C
NR_132403.1:n.777A>C
NR_132404.1:n.777A>C
NR_132405.1:n.773A>C
NR_132406.1:n.686-272A>C
NR_132407.1:n.541A>C
NR_132408.1:n.537A>C
NR_132409.1:n.398A>C
NR_132410.1:n.446-272A>C
NR_132412.1:n.307-272A>C
NR_132413.1:n.195-2929A>C
NR_132414.1:n.195-5656A>C
NR_132415.1:n.1014A>C
XM_005270954.1:c.664A>C	XP_005271011.1:p.Ser222Arg
XM_006710706.1:c.484A>C	XP_006710769.1:p.Ser162Arg
XM_005270954.2:c.664A>C	XP_005271011.1:p.Ser222Arg
XR_946672.2:n.1007A>C
NM_017646.6:c.907A>C MANE Select	NP_060116.2:p.Ser303Arg