Canonical Allele Identifier: CA339832759

Gene: TRIT1

Linked Data

• MyVariant Identifiers: chr1:g.40312935A>C (hg19) ; chr1:g.39847263A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.39847263A>C , CM000663.2:g.39847263A>C	GRCh38
NC_000001.10:g.40312935A>C , CM000663.1:g.40312935A>C	GRCh37
NC_000001.9:g.40085522A>C	NCBI36
NG_042822.1:g.41249T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000316891.10:c.963T>G MANE Select	ENSP00000321810.5:p.Tyr321Ter
ENST00000648678.1:c.1855T>G	ENSP00000497805.1:n.1855T>G
ENST00000316891.9:c.963T>G	ENSP00000321810.5:p.Tyr321Ter
ENST00000372818.5:c.928+285T>G	ENSP00000361905.1:n.928+285T>G
ENST00000441669.6:c.717T>G	ENSP00000388333.2:p.Tyr239Ter
ENST00000462797.5:c.963T>G	ENSP00000473773.1:p.Tyr321Ter
ENST00000465417.5:n.147T>G
ENST00000467774.1:n.245T>G
ENST00000489945.5:c.*381T>G	ENSP00000473745.1:n.*381T>G
ENST00000491865.5:n.198T>G
ENST00000492612.6:c.807T>G
ENST00000495175.6:c.*385T>G	ENSP00000474264.1:n.*385T>G
ENST00000537440.5:c.51T>G	ENSP00000437700.1:p.Tyr17Ter
ENST00000541099.5:c.-140-2623T>G	ENSP00000437896.1:n.-140-2623T>G
NM_001312691.1:c.928+285T>G	NP_001299620.1:n.928+285T>G
NM_001312692.1:c.717T>G	NP_001299621.1:p.Tyr239Ter
NM_017646.4:c.963T>G	NP_060116.2:p.Tyr321Ter
NM_017646.5:c.963T>G	NP_060116.2:p.Tyr321Ter
NR_132401.1:n.979T>G
NR_132402.1:n.837T>G
NR_132403.1:n.833T>G
NR_132404.1:n.833T>G
NR_132405.1:n.829T>G
NR_132406.1:n.720T>G
NR_132407.1:n.597T>G
NR_132408.1:n.593T>G
NR_132409.1:n.454T>G
NR_132410.1:n.480T>G
NR_132412.1:n.341T>G
NR_132413.1:n.195-2623T>G
NR_132414.1:n.195-5350T>G
NR_132415.1:n.1070T>G
XM_005270954.1:c.720T>G	XP_005271011.1:p.Tyr240Ter
XM_006710706.1:c.540T>G	XP_006710769.1:p.Tyr180Ter
XM_005270954.2:c.720T>G	XP_005271011.1:p.Tyr240Ter
XR_946672.2:n.1063T>G
NM_017646.6:c.963T>G MANE Select	NP_060116.2:p.Tyr321Ter