Canonical Allele Identifier: CA1146918350

Gene: TRIT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.39847052C= , CM000663.2:g.39847052C=	GRCh38
NC_000001.10:g.40312724C= , CM000663.1:g.40312724C=	GRCh37
NC_000001.9:g.40085311C=	NCBI36
NG_042822.1:g.41460G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316891.10:c.1006+168G= MANE Select	ENSP00000321810.5:n.1006+168G=
ENST00000648678.1:c.1898+168G=	ENSP00000497805.1:n.1898+168G=
ENST00000316891.9:c.1006+168G=	ENSP00000321810.5:n.1006+168G=
ENST00000372818.5:c.928+496G=	ENSP00000361905.1:n.928+496G=
ENST00000441669.6:c.760+168G=	ENSP00000388333.2:n.760+168G=
ENST00000462797.5:c.1006+168G=	ENSP00000473773.1:n.1006+168G=
ENST00000465417.5:n.190+168G=
ENST00000467774.1:n.456G=
ENST00000491865.5:n.241+168G=
ENST00000492612.6:c.850+168G=
ENST00000495175.6:c.*428+168G=	ENSP00000474264.1:n.*428+168G=
ENST00000537440.5:c.94+168G=	ENSP00000437700.1:n.94+168G=
ENST00000541099.5:c.-140-2412G=	ENSP00000437896.1:n.-140-2412G=
NM_001312691.1:c.928+496G=	NP_001299620.1:n.928+496G=
NM_001312692.1:c.760+168G=	NP_001299621.1:n.760+168G=
NM_017646.4:c.1006+168G=	NP_060116.2:n.1006+168G=
NM_017646.5:c.1006+168G=	NP_060116.2:n.1006+168G=
NR_132401.1:n.1022+168G=
NR_132402.1:n.880+168G=
NR_132403.1:n.876+168G=
NR_132404.1:n.876+168G=
NR_132405.1:n.872+168G=
NR_132406.1:n.763+168G=
NR_132407.1:n.640+168G=
NR_132408.1:n.636+168G=
NR_132409.1:n.497+168G=
NR_132410.1:n.523+168G=
NR_132412.1:n.384+168G=
NR_132413.1:n.195-2412G=
NR_132414.1:n.195-5139G=
NR_132415.1:n.1113+168G=
XM_005270954.1:c.763+168G=	XP_005271011.1:n.763+168G=
XM_006710706.1:c.583+168G=	XP_006710769.1:n.583+168G=
XM_005270954.2:c.763+168G=	XP_005271011.1:n.763+168G=
XR_946672.2:n.1106+168G=
NM_017646.6:c.1006+168G= MANE Select	NP_060116.2:n.1006+168G=