Canonical Allele Identifier: CA339833269

Gene: TRIT1

Linked Data

• MyVariant Identifiers: chr1:g.40313240C>G (hg19) ; chr1:g.39847568C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.39847568C>G , CM000663.2:g.39847568C>G	GRCh38
NC_000001.10:g.40313240C>G , CM000663.1:g.40313240C>G	GRCh37
NC_000001.9:g.40085827C>G	NCBI36
NG_042822.1:g.40944G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316891.10:c.908G>C MANE Select	ENSP00000321810.5:p.Ser303Thr
ENST00000648678.1:c.1800G>C	ENSP00000497805.1:n.1800G>C
ENST00000316891.9:c.908G>C	ENSP00000321810.5:p.Ser303Thr
ENST00000372818.5:c.908G>C	ENSP00000361905.1:p.Ser303Thr
ENST00000441669.6:c.662G>C	ENSP00000388333.2:p.Ser221Thr
ENST00000462797.5:c.908G>C	ENSP00000473773.1:p.Ser303Thr
ENST00000465417.5:n.113-271G>C
ENST00000467774.1:n.190G>C
ENST00000486825.6:c.813G>C
ENST00000489945.5:c.*326G>C	ENSP00000473745.1:n.*326G>C
ENST00000491865.5:n.164-271G>C
ENST00000492612.6:c.752G>C
ENST00000495175.6:c.*330G>C	ENSP00000474264.1:n.*330G>C
ENST00000537440.5:c.17-271G>C	ENSP00000437700.1:n.17-271G>C
ENST00000541099.5:c.-140-2928G>C	ENSP00000437896.1:n.-140-2928G>C
NM_001312691.1:c.908G>C	NP_001299620.1:p.Ser303Thr
NM_001312692.1:c.662G>C	NP_001299621.1:p.Ser221Thr
NM_017646.4:c.908G>C	NP_060116.2:p.Ser303Thr
NM_017646.5:c.908G>C	NP_060116.2:p.Ser303Thr
NR_132401.1:n.924G>C
NR_132402.1:n.782G>C
NR_132403.1:n.778G>C
NR_132404.1:n.778G>C
NR_132405.1:n.774G>C
NR_132406.1:n.686-271G>C
NR_132407.1:n.542G>C
NR_132408.1:n.538G>C
NR_132409.1:n.399G>C
NR_132410.1:n.446-271G>C
NR_132412.1:n.307-271G>C
NR_132413.1:n.195-2928G>C
NR_132414.1:n.195-5655G>C
NR_132415.1:n.1015G>C
XM_005270954.1:c.665G>C	XP_005271011.1:p.Ser222Thr
XM_006710706.1:c.485G>C	XP_006710769.1:p.Ser162Thr
XM_005270954.2:c.665G>C	XP_005271011.1:p.Ser222Thr
XR_946672.2:n.1008G>C
NM_017646.6:c.908G>C MANE Select	NP_060116.2:p.Ser303Thr