Canonical Allele Identifier: CA339833267

Gene: TRIT1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316891.10:c.908G>A MANE Select	ENSP00000321810.5:p.Ser303Asn
ENST00000648678.1:c.1800G>A	ENSP00000497805.1:n.1800G>A
ENST00000316891.9:c.908G>A	ENSP00000321810.5:p.Ser303Asn
ENST00000372818.5:c.908G>A	ENSP00000361905.1:p.Ser303Asn
ENST00000441669.6:c.662G>A	ENSP00000388333.2:p.Ser221Asn
ENST00000462797.5:c.908G>A	ENSP00000473773.1:p.Ser303Asn
ENST00000465417.5:n.113-271G>A
ENST00000467774.1:n.190G>A
ENST00000486825.6:c.813G>A
ENST00000489945.5:c.*326G>A	ENSP00000473745.1:n.*326G>A
ENST00000491865.5:n.164-271G>A
ENST00000492612.6:c.752G>A
ENST00000495175.6:c.*330G>A	ENSP00000474264.1:n.*330G>A
ENST00000537440.5:c.17-271G>A	ENSP00000437700.1:n.17-271G>A
ENST00000541099.5:c.-140-2928G>A	ENSP00000437896.1:n.-140-2928G>A
NM_001312691.1:c.908G>A	NP_001299620.1:p.Ser303Asn
NM_001312692.1:c.662G>A	NP_001299621.1:p.Ser221Asn
NM_017646.4:c.908G>A	NP_060116.2:p.Ser303Asn
NM_017646.5:c.908G>A	NP_060116.2:p.Ser303Asn
NR_132401.1:n.924G>A
NR_132402.1:n.782G>A
NR_132403.1:n.778G>A
NR_132404.1:n.778G>A
NR_132405.1:n.774G>A
NR_132406.1:n.686-271G>A
NR_132407.1:n.542G>A
NR_132408.1:n.538G>A
NR_132409.1:n.399G>A
NR_132410.1:n.446-271G>A
NR_132412.1:n.307-271G>A
NR_132413.1:n.195-2928G>A
NR_132414.1:n.195-5655G>A
NR_132415.1:n.1015G>A
XM_005270954.1:c.665G>A	XP_005271011.1:p.Ser222Asn
XM_006710706.1:c.485G>A	XP_006710769.1:p.Ser162Asn
XM_005270954.2:c.665G>A	XP_005271011.1:p.Ser222Asn
XR_946672.2:n.1008G>A
NM_017646.6:c.908G>A MANE Select	NP_060116.2:p.Ser303Asn