Canonical Allele Identifier: CA339832775

Gene: TRIT1

Linked Data

• MyVariant Identifiers: chr1:g.40312937A>C (hg19) ; chr1:g.39847265A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.39847265A>C , CM000663.2:g.39847265A>C	GRCh38
NC_000001.10:g.40312937A>C , CM000663.1:g.40312937A>C	GRCh37
NC_000001.9:g.40085524A>C	NCBI36
NG_042822.1:g.41247T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000316891.10:c.961T>G MANE Select	ENSP00000321810.5:p.Tyr321Asp
ENST00000648678.1:c.1853T>G	ENSP00000497805.1:n.1853T>G
ENST00000316891.9:c.961T>G	ENSP00000321810.5:p.Tyr321Asp
ENST00000372818.5:c.928+283T>G	ENSP00000361905.1:n.928+283T>G
ENST00000441669.6:c.715T>G	ENSP00000388333.2:p.Tyr239Asp
ENST00000462797.5:c.961T>G	ENSP00000473773.1:p.Tyr321Asp
ENST00000465417.5:n.145T>G
ENST00000467774.1:n.243T>G
ENST00000489945.5:c.*379T>G	ENSP00000473745.1:n.*379T>G
ENST00000491865.5:n.196T>G
ENST00000492612.6:c.805T>G
ENST00000495175.6:c.*383T>G	ENSP00000474264.1:n.*383T>G
ENST00000537440.5:c.49T>G	ENSP00000437700.1:p.Tyr17Asp
ENST00000541099.5:c.-140-2625T>G	ENSP00000437896.1:n.-140-2625T>G
NM_001312691.1:c.928+283T>G	NP_001299620.1:n.928+283T>G
NM_001312692.1:c.715T>G	NP_001299621.1:p.Tyr239Asp
NM_017646.4:c.961T>G	NP_060116.2:p.Tyr321Asp
NM_017646.5:c.961T>G	NP_060116.2:p.Tyr321Asp
NR_132401.1:n.977T>G
NR_132402.1:n.835T>G
NR_132403.1:n.831T>G
NR_132404.1:n.831T>G
NR_132405.1:n.827T>G
NR_132406.1:n.718T>G
NR_132407.1:n.595T>G
NR_132408.1:n.591T>G
NR_132409.1:n.452T>G
NR_132410.1:n.478T>G
NR_132412.1:n.339T>G
NR_132413.1:n.195-2625T>G
NR_132414.1:n.195-5352T>G
NR_132415.1:n.1068T>G
XM_005270954.1:c.718T>G	XP_005271011.1:p.Tyr240Asp
XM_006710706.1:c.538T>G	XP_006710769.1:p.Tyr180Asp
XM_005270954.2:c.718T>G	XP_005271011.1:p.Tyr240Asp
XR_946672.2:n.1061T>G
NM_017646.6:c.961T>G MANE Select	NP_060116.2:p.Tyr321Asp