Canonical Allele Identifier: CA1143518838

Gene: TRIT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.39847246C= , CM000663.2:g.39847246C=	GRCh38
NC_000001.10:g.40312918C= , CM000663.1:g.40312918C=	GRCh37
NC_000001.9:g.40085505C=	NCBI36
NG_042822.1:g.41266G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316891.10:c.980G= MANE Select	ENSP00000321810.5:p.Arg327=
ENST00000648678.1:c.1872G=	ENSP00000497805.1:n.1872G=
ENST00000316891.9:c.980G=	ENSP00000321810.5:p.Arg327=
ENST00000372818.5:c.928+302G=	ENSP00000361905.1:n.928+302G=
ENST00000441669.6:c.734G=	ENSP00000388333.2:p.Arg245=
ENST00000462797.5:c.980G=	ENSP00000473773.1:p.Arg327=
ENST00000465417.5:n.164G=
ENST00000467774.1:n.262G=
ENST00000489945.5:c.*398G=	ENSP00000473745.1:n.*398G=
ENST00000491865.5:n.215G=
ENST00000492612.6:c.824G=
ENST00000495175.6:c.*402G=	ENSP00000474264.1:n.*402G=
ENST00000537440.5:c.68G=	ENSP00000437700.1:p.Arg23=
ENST00000541099.5:c.-140-2606G=	ENSP00000437896.1:n.-140-2606G=
NM_001312691.1:c.928+302G=	NP_001299620.1:n.928+302G=
NM_001312692.1:c.734G=	NP_001299621.1:p.Arg245=
NM_017646.4:c.980G=	NP_060116.2:p.Arg327=
NM_017646.5:c.980G=	NP_060116.2:p.Arg327=
NR_132401.1:n.996G=
NR_132402.1:n.854G=
NR_132403.1:n.850G=
NR_132404.1:n.850G=
NR_132405.1:n.846G=
NR_132406.1:n.737G=
NR_132407.1:n.614G=
NR_132408.1:n.610G=
NR_132409.1:n.471G=
NR_132410.1:n.497G=
NR_132412.1:n.358G=
NR_132413.1:n.195-2606G=
NR_132414.1:n.195-5333G=
NR_132415.1:n.1087G=
XM_005270954.1:c.737G=	XP_005271011.1:p.Arg246=
XM_006710706.1:c.557G=	XP_006710769.1:p.Arg186=
XM_005270954.2:c.737G=	XP_005271011.1:p.Arg246=
XR_946672.2:n.1080G=
NM_017646.6:c.980G= MANE Select	NP_060116.2:p.Arg327=