Canonical Allele Identifier: CA1164144218

Gene: TRIT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.39847232G= , CM000663.2:g.39847232G=	GRCh38
NC_000001.10:g.40312904G= , CM000663.1:g.40312904G=	GRCh37
NC_000001.9:g.40085491G=	NCBI36
NG_042822.1:g.41280C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316891.10:c.994C= MANE Select	ENSP00000321810.5:p.Arg332=
ENST00000648678.1:c.1886C=	ENSP00000497805.1:n.1886C=
ENST00000316891.9:c.994C=	ENSP00000321810.5:p.Arg332=
ENST00000372818.5:c.928+316C=	ENSP00000361905.1:n.928+316C=
ENST00000441669.6:c.748C=	ENSP00000388333.2:p.Arg250=
ENST00000462797.5:c.994C=	ENSP00000473773.1:p.Arg332=
ENST00000465417.5:n.178C=
ENST00000467774.1:n.276C=
ENST00000489945.5:c.*412C=	ENSP00000473745.1:n.*412C=
ENST00000491865.5:n.229C=
ENST00000492612.6:c.838C=
ENST00000495175.6:c.*416C=	ENSP00000474264.1:n.*416C=
ENST00000537440.5:c.82C=	ENSP00000437700.1:p.Arg28=
ENST00000541099.5:c.-140-2592C=	ENSP00000437896.1:n.-140-2592C=
NM_001312691.1:c.928+316C=	NP_001299620.1:n.928+316C=
NM_001312692.1:c.748C=	NP_001299621.1:p.Arg250=
NM_017646.4:c.994C=	NP_060116.2:p.Arg332=
NM_017646.5:c.994C=	NP_060116.2:p.Arg332=
NR_132401.1:n.1010C=
NR_132402.1:n.868C=
NR_132403.1:n.864C=
NR_132404.1:n.864C=
NR_132405.1:n.860C=
NR_132406.1:n.751C=
NR_132407.1:n.628C=
NR_132408.1:n.624C=
NR_132409.1:n.485C=
NR_132410.1:n.511C=
NR_132412.1:n.372C=
NR_132413.1:n.195-2592C=
NR_132414.1:n.195-5319C=
NR_132415.1:n.1101C=
XM_005270954.1:c.751C=	XP_005271011.1:p.Arg251=
XM_006710706.1:c.571C=	XP_006710769.1:p.Arg191=
XM_005270954.2:c.751C=	XP_005271011.1:p.Arg251=
XR_946672.2:n.1094C=
NM_017646.6:c.994C= MANE Select	NP_060116.2:p.Arg332=