Canonical Allele Identifier: CA339832605

Gene: TRIT1

Linked Data

• MyVariant Identifiers: chr1:g.40312912A>T (hg19) ; chr1:g.39847240A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.39847240A>T , CM000663.2:g.39847240A>T	GRCh38
NC_000001.10:g.40312912A>T , CM000663.1:g.40312912A>T	GRCh37
NC_000001.9:g.40085499A>T	NCBI36
NG_042822.1:g.41272T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316891.10:c.986T>A MANE Select	ENSP00000321810.5:p.Val329Asp
ENST00000648678.1:c.1878T>A	ENSP00000497805.1:n.1878T>A
ENST00000316891.9:c.986T>A	ENSP00000321810.5:p.Val329Asp
ENST00000372818.5:c.928+308T>A	ENSP00000361905.1:n.928+308T>A
ENST00000441669.6:c.740T>A	ENSP00000388333.2:p.Val247Asp
ENST00000462797.5:c.986T>A	ENSP00000473773.1:p.Val329Asp
ENST00000465417.5:n.170T>A
ENST00000467774.1:n.268T>A
ENST00000489945.5:c.*404T>A	ENSP00000473745.1:n.*404T>A
ENST00000491865.5:n.221T>A
ENST00000492612.6:c.830T>A
ENST00000495175.6:c.*408T>A	ENSP00000474264.1:n.*408T>A
ENST00000537440.5:c.74T>A	ENSP00000437700.1:p.Val25Asp
ENST00000541099.5:c.-140-2600T>A	ENSP00000437896.1:n.-140-2600T>A
NM_001312691.1:c.928+308T>A	NP_001299620.1:n.928+308T>A
NM_001312692.1:c.740T>A	NP_001299621.1:p.Val247Asp
NM_017646.4:c.986T>A	NP_060116.2:p.Val329Asp
NM_017646.5:c.986T>A	NP_060116.2:p.Val329Asp
NR_132401.1:n.1002T>A
NR_132402.1:n.860T>A
NR_132403.1:n.856T>A
NR_132404.1:n.856T>A
NR_132405.1:n.852T>A
NR_132406.1:n.743T>A
NR_132407.1:n.620T>A
NR_132408.1:n.616T>A
NR_132409.1:n.477T>A
NR_132410.1:n.503T>A
NR_132412.1:n.364T>A
NR_132413.1:n.195-2600T>A
NR_132414.1:n.195-5327T>A
NR_132415.1:n.1093T>A
XM_005270954.1:c.743T>A	XP_005271011.1:p.Val248Asp
XM_006710706.1:c.563T>A	XP_006710769.1:p.Val188Asp
XM_005270954.2:c.743T>A	XP_005271011.1:p.Val248Asp
XR_946672.2:n.1086T>A
NM_017646.6:c.986T>A MANE Select	NP_060116.2:p.Val329Asp