Canonical Allele Identifier: CA1141167798

Gene: TRIT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.39847192A= , CM000663.2:g.39847192A=	GRCh38
NC_000001.10:g.40312864A= , CM000663.1:g.40312864A=	GRCh37
NC_000001.9:g.40085451A=	NCBI36
NG_042822.1:g.41320T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316891.10:c.1006+28T= MANE Select	ENSP00000321810.5:n.1006+28T=
ENST00000648678.1:c.1898+28T=	ENSP00000497805.1:n.1898+28T=
ENST00000316891.9:c.1006+28T=	ENSP00000321810.5:n.1006+28T=
ENST00000372818.5:c.928+356T=	ENSP00000361905.1:n.928+356T=
ENST00000441669.6:c.760+28T=	ENSP00000388333.2:n.760+28T=
ENST00000462797.5:c.1006+28T=	ENSP00000473773.1:n.1006+28T=
ENST00000465417.5:n.190+28T=
ENST00000467774.1:n.316T=
ENST00000491865.5:n.241+28T=
ENST00000492612.6:c.850+28T=
ENST00000495175.6:c.*428+28T=	ENSP00000474264.1:n.*428+28T=
ENST00000537440.5:c.94+28T=	ENSP00000437700.1:n.94+28T=
ENST00000541099.5:c.-140-2552T=	ENSP00000437896.1:n.-140-2552T=
NM_001312691.1:c.928+356T=	NP_001299620.1:n.928+356T=
NM_001312692.1:c.760+28T=	NP_001299621.1:n.760+28T=
NM_017646.4:c.1006+28T=	NP_060116.2:n.1006+28T=
NM_017646.5:c.1006+28T=	NP_060116.2:n.1006+28T=
NR_132401.1:n.1022+28T=
NR_132402.1:n.880+28T=
NR_132403.1:n.876+28T=
NR_132404.1:n.876+28T=
NR_132405.1:n.872+28T=
NR_132406.1:n.763+28T=
NR_132407.1:n.640+28T=
NR_132408.1:n.636+28T=
NR_132409.1:n.497+28T=
NR_132410.1:n.523+28T=
NR_132412.1:n.384+28T=
NR_132413.1:n.195-2552T=
NR_132414.1:n.195-5279T=
NR_132415.1:n.1113+28T=
XM_005270954.1:c.763+28T=	XP_005271011.1:n.763+28T=
XM_006710706.1:c.583+28T=	XP_006710769.1:n.583+28T=
XM_005270954.2:c.763+28T=	XP_005271011.1:n.763+28T=
XR_946672.2:n.1106+28T=
NM_017646.6:c.1006+28T= MANE Select	NP_060116.2:n.1006+28T=