Canonical Allele Identifier: CA1164144212

Gene: TRIT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.39847224C= , CM000663.2:g.39847224C=	GRCh38
NC_000001.10:g.40312896C= , CM000663.1:g.40312896C=	GRCh37
NC_000001.9:g.40085483C=	NCBI36
NG_042822.1:g.41288G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316891.10:c.1002G= MANE Select	ENSP00000321810.5:p.Leu334=
ENST00000648678.1:c.1894G=	ENSP00000497805.1:n.1894G=
ENST00000316891.9:c.1002G=	ENSP00000321810.5:p.Leu334=
ENST00000372818.5:c.928+324G=	ENSP00000361905.1:n.928+324G=
ENST00000441669.6:c.756G=	ENSP00000388333.2:p.Leu252=
ENST00000462797.5:c.1002G=	ENSP00000473773.1:p.Leu334=
ENST00000465417.5:n.186G=
ENST00000467774.1:n.284G=
ENST00000489945.5:c.*420G=	ENSP00000473745.1:n.*420G=
ENST00000491865.5:n.237G=
ENST00000492612.6:c.846G=
ENST00000495175.6:c.*424G=	ENSP00000474264.1:n.*424G=
ENST00000537440.5:c.90G=	ENSP00000437700.1:p.Leu30=
ENST00000541099.5:c.-140-2584G=	ENSP00000437896.1:n.-140-2584G=
NM_001312691.1:c.928+324G=	NP_001299620.1:n.928+324G=
NM_001312692.1:c.756G=	NP_001299621.1:p.Leu252=
NM_017646.4:c.1002G=	NP_060116.2:p.Leu334=
NM_017646.5:c.1002G=	NP_060116.2:p.Leu334=
NR_132401.1:n.1018G=
NR_132402.1:n.876G=
NR_132403.1:n.872G=
NR_132404.1:n.872G=
NR_132405.1:n.868G=
NR_132406.1:n.759G=
NR_132407.1:n.636G=
NR_132408.1:n.632G=
NR_132409.1:n.493G=
NR_132410.1:n.519G=
NR_132412.1:n.380G=
NR_132413.1:n.195-2584G=
NR_132414.1:n.195-5311G=
NR_132415.1:n.1109G=
XM_005270954.1:c.759G=	XP_005271011.1:p.Leu253=
XM_006710706.1:c.579G=	XP_006710769.1:p.Leu193=
XM_005270954.2:c.759G=	XP_005271011.1:p.Leu253=
XR_946672.2:n.1102G=
NM_017646.6:c.1002G= MANE Select	NP_060116.2:p.Leu334=