Canonical Allele Identifier: CA1164144333

Gene: TRIT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.39847323C= , CM000663.2:g.39847323C=	GRCh38
NC_000001.10:g.40312995C= , CM000663.1:g.40312995C=	GRCh37
NC_000001.9:g.40085582C=	NCBI36
NG_042822.1:g.41189G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316891.10:c.929-26G= MANE Select	ENSP00000321810.5:n.929-26G=
ENST00000648678.1:c.1821-26G=	ENSP00000497805.1:n.1821-26G=
ENST00000316891.9:c.929-26G=	ENSP00000321810.5:n.929-26G=
ENST00000372818.5:c.928+225G=	ENSP00000361905.1:n.928+225G=
ENST00000441669.6:c.683-26G=	ENSP00000388333.2:n.683-26G=
ENST00000462797.5:c.929-26G=	ENSP00000473773.1:n.929-26G=
ENST00000465417.5:n.113-26G=
ENST00000467774.1:n.211-26G=
ENST00000486825.6:c.834-26G=
ENST00000489945.5:c.*347-26G=	ENSP00000473745.1:n.*347-26G=
ENST00000491865.5:n.164-26G=
ENST00000492612.6:c.773-26G=
ENST00000495175.6:c.*351-26G=	ENSP00000474264.1:n.*351-26G=
ENST00000537440.5:c.17-26G=	ENSP00000437700.1:n.17-26G=
ENST00000541099.5:c.-140-2683G=	ENSP00000437896.1:n.-140-2683G=
NM_001312691.1:c.928+225G=	NP_001299620.1:n.928+225G=
NM_001312692.1:c.683-26G=	NP_001299621.1:n.683-26G=
NM_017646.4:c.929-26G=	NP_060116.2:n.929-26G=
NM_017646.5:c.929-26G=	NP_060116.2:n.929-26G=
NR_132401.1:n.945-26G=
NR_132402.1:n.803-26G=
NR_132403.1:n.799-26G=
NR_132404.1:n.799-26G=
NR_132405.1:n.795-26G=
NR_132406.1:n.686-26G=
NR_132407.1:n.563-26G=
NR_132408.1:n.559-26G=
NR_132409.1:n.420-26G=
NR_132410.1:n.446-26G=
NR_132412.1:n.307-26G=
NR_132413.1:n.195-2683G=
NR_132414.1:n.195-5410G=
NR_132415.1:n.1036-26G=
XM_005270954.1:c.686-26G=	XP_005271011.1:n.686-26G=
XM_006710706.1:c.506-26G=	XP_006710769.1:n.506-26G=
XM_005270954.2:c.686-26G=	XP_005271011.1:n.686-26G=
XR_946672.2:n.1029-26G=
NM_017646.6:c.929-26G= MANE Select	NP_060116.2:n.929-26G=