Canonical Allele Identifier: CA417302030

Gene: TRIT1

Linked Data

• MyVariant Identifiers: chr1:g.40313239A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.39847567A>G , CM000663.2:g.39847567A>G	GRCh38
NC_000001.10:g.40313239A>G , CM000663.1:g.40313239A>G	GRCh37
NC_000001.9:g.40085826A>G	NCBI36
NG_042822.1:g.40945T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316891.10:c.909T>C MANE Select	ENSP00000321810.5:p.Ser303=
ENST00000648678.1:c.1801T>C	ENSP00000497805.1:n.1801T>C
ENST00000316891.9:c.909T>C	ENSP00000321810.5:p.Ser303=
ENST00000372818.5:c.909T>C	ENSP00000361905.1:p.Ser303=
ENST00000441669.6:c.663T>C	ENSP00000388333.2:p.Ser221=
ENST00000462797.5:c.909T>C	ENSP00000473773.1:p.Ser303=
ENST00000465417.5:n.113-270T>C
ENST00000467774.1:n.191T>C
ENST00000486825.6:c.814T>C
ENST00000489945.5:c.*327T>C	ENSP00000473745.1:n.*327T>C
ENST00000491865.5:n.164-270T>C
ENST00000492612.6:c.753T>C
ENST00000495175.6:c.*331T>C	ENSP00000474264.1:n.*331T>C
ENST00000537440.5:c.17-270T>C	ENSP00000437700.1:n.17-270T>C
ENST00000541099.5:c.-140-2927T>C	ENSP00000437896.1:n.-140-2927T>C
NM_001312691.1:c.909T>C	NP_001299620.1:p.Ser303=
NM_001312692.1:c.663T>C	NP_001299621.1:p.Ser221=
NM_017646.4:c.909T>C	NP_060116.2:p.Ser303=
NM_017646.5:c.909T>C	NP_060116.2:p.Ser303=
NR_132401.1:n.925T>C
NR_132402.1:n.783T>C
NR_132403.1:n.779T>C
NR_132404.1:n.779T>C
NR_132405.1:n.775T>C
NR_132406.1:n.686-270T>C
NR_132407.1:n.543T>C
NR_132408.1:n.539T>C
NR_132409.1:n.400T>C
NR_132410.1:n.446-270T>C
NR_132412.1:n.307-270T>C
NR_132413.1:n.195-2927T>C
NR_132414.1:n.195-5654T>C
NR_132415.1:n.1016T>C
XM_005270954.1:c.666T>C	XP_005271011.1:p.Ser222=
XM_006710706.1:c.486T>C	XP_006710769.1:p.Ser162=
XM_005270954.2:c.666T>C	XP_005271011.1:p.Ser222=
XR_946672.2:n.1009T>C
NM_017646.6:c.909T>C MANE Select	NP_060116.2:p.Ser303=