Canonical Allele Identifier: CA339832977

Gene: TRIT1

Linked Data

• MyVariant Identifiers: chr1:g.40312965A>C (hg19) ; chr1:g.39847293A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.39847293A>C , CM000663.2:g.39847293A>C	GRCh38
NC_000001.10:g.40312965A>C , CM000663.1:g.40312965A>C	GRCh37
NC_000001.9:g.40085552A>C	NCBI36
NG_042822.1:g.41219T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316891.10:c.933T>G MANE Select	ENSP00000321810.5:p.Ile311Met
ENST00000648678.1:c.1825T>G	ENSP00000497805.1:n.1825T>G
ENST00000316891.9:c.933T>G	ENSP00000321810.5:p.Ile311Met
ENST00000372818.5:c.928+255T>G	ENSP00000361905.1:n.928+255T>G
ENST00000441669.6:c.687T>G	ENSP00000388333.2:p.Ile229Met
ENST00000462797.5:c.933T>G	ENSP00000473773.1:p.Ile311Met
ENST00000465417.5:n.117T>G
ENST00000467774.1:n.215T>G
ENST00000486825.6:c.838T>G
ENST00000489945.5:c.*351T>G	ENSP00000473745.1:n.*351T>G
ENST00000491865.5:n.168T>G
ENST00000492612.6:c.777T>G
ENST00000495175.6:c.*355T>G	ENSP00000474264.1:n.*355T>G
ENST00000537440.5:c.21T>G	ENSP00000437700.1:p.Ile7Met
ENST00000541099.5:c.-140-2653T>G	ENSP00000437896.1:n.-140-2653T>G
NM_001312691.1:c.928+255T>G	NP_001299620.1:n.928+255T>G
NM_001312692.1:c.687T>G	NP_001299621.1:p.Ile229Met
NM_017646.4:c.933T>G	NP_060116.2:p.Ile311Met
NM_017646.5:c.933T>G	NP_060116.2:p.Ile311Met
NR_132401.1:n.949T>G
NR_132402.1:n.807T>G
NR_132403.1:n.803T>G
NR_132404.1:n.803T>G
NR_132405.1:n.799T>G
NR_132406.1:n.690T>G
NR_132407.1:n.567T>G
NR_132408.1:n.563T>G
NR_132409.1:n.424T>G
NR_132410.1:n.450T>G
NR_132412.1:n.311T>G
NR_132413.1:n.195-2653T>G
NR_132414.1:n.195-5380T>G
NR_132415.1:n.1040T>G
XM_005270954.1:c.690T>G	XP_005271011.1:p.Ile230Met
XM_006710706.1:c.510T>G	XP_006710769.1:p.Ile170Met
XM_005270954.2:c.690T>G	XP_005271011.1:p.Ile230Met
XR_946672.2:n.1033T>G
NM_017646.6:c.933T>G MANE Select	NP_060116.2:p.Ile311Met