Canonical Allele Identifier: CA1164144419

Gene: TRIT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.39847459T= , CM000663.2:g.39847459T=	GRCh38
NC_000001.10:g.40313131T= , CM000663.1:g.40313131T=	GRCh37
NC_000001.9:g.40085718T=	NCBI36
NG_042822.1:g.41053A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316891.10:c.928+89A= MANE Select	ENSP00000321810.5:n.928+89A=
ENST00000648678.1:c.1820+89A=	ENSP00000497805.1:n.1820+89A=
ENST00000316891.9:c.928+89A=	ENSP00000321810.5:n.928+89A=
ENST00000372818.5:c.928+89A=	ENSP00000361905.1:n.928+89A=
ENST00000441669.6:c.682+89A=	ENSP00000388333.2:n.682+89A=
ENST00000462797.5:c.928+89A=	ENSP00000473773.1:n.928+89A=
ENST00000465417.5:n.113-162A=
ENST00000467774.1:n.210+89A=
ENST00000486825.6:c.833+89A=
ENST00000489945.5:c.*346+89A=	ENSP00000473745.1:n.*346+89A=
ENST00000491865.5:n.164-162A=
ENST00000492612.6:c.772+89A=
ENST00000495175.6:c.*350+89A=	ENSP00000474264.1:n.*350+89A=
ENST00000537440.5:c.17-162A=	ENSP00000437700.1:n.17-162A=
ENST00000541099.5:c.-140-2819A=	ENSP00000437896.1:n.-140-2819A=
NM_001312691.1:c.928+89A=	NP_001299620.1:n.928+89A=
NM_001312692.1:c.682+89A=	NP_001299621.1:n.682+89A=
NM_017646.4:c.928+89A=	NP_060116.2:n.928+89A=
NM_017646.5:c.928+89A=	NP_060116.2:n.928+89A=
NR_132401.1:n.944+89A=
NR_132402.1:n.802+89A=
NR_132403.1:n.798+89A=
NR_132404.1:n.798+89A=
NR_132405.1:n.794+89A=
NR_132406.1:n.686-162A=
NR_132407.1:n.562+89A=
NR_132408.1:n.558+89A=
NR_132409.1:n.419+89A=
NR_132410.1:n.446-162A=
NR_132412.1:n.307-162A=
NR_132413.1:n.195-2819A=
NR_132414.1:n.195-5546A=
NR_132415.1:n.1035+89A=
XM_005270954.1:c.685+89A=	XP_005271011.1:n.685+89A=
XM_006710706.1:c.505+89A=	XP_006710769.1:n.505+89A=
XM_005270954.2:c.685+89A=	XP_005271011.1:n.685+89A=
XR_946672.2:n.1028+89A=
NM_017646.6:c.928+89A= MANE Select	NP_060116.2:n.928+89A=