Canonical Allele Identifier: CA339833255

Gene: TRIT1

Linked Data

• MyVariant Identifiers: chr1:g.40313238T>G (hg19) ; chr1:g.39847566T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.39847566T>G , CM000663.2:g.39847566T>G	GRCh38
NC_000001.10:g.40313238T>G , CM000663.1:g.40313238T>G	GRCh37
NC_000001.9:g.40085825T>G	NCBI36
NG_042822.1:g.40946A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316891.10:c.910A>C MANE Select	ENSP00000321810.5:p.Asn304His
ENST00000648678.1:c.1802A>C	ENSP00000497805.1:n.1802A>C
ENST00000316891.9:c.910A>C	ENSP00000321810.5:p.Asn304His
ENST00000372818.5:c.910A>C	ENSP00000361905.1:p.Asn304His
ENST00000441669.6:c.664A>C	ENSP00000388333.2:p.Asn222His
ENST00000462797.5:c.910A>C	ENSP00000473773.1:p.Asn304His
ENST00000465417.5:n.113-269A>C
ENST00000467774.1:n.192A>C
ENST00000486825.6:c.815A>C
ENST00000489945.5:c.*328A>C	ENSP00000473745.1:n.*328A>C
ENST00000491865.5:n.164-269A>C
ENST00000492612.6:c.754A>C
ENST00000495175.6:c.*332A>C	ENSP00000474264.1:n.*332A>C
ENST00000537440.5:c.17-269A>C	ENSP00000437700.1:n.17-269A>C
ENST00000541099.5:c.-140-2926A>C	ENSP00000437896.1:n.-140-2926A>C
NM_001312691.1:c.910A>C	NP_001299620.1:p.Asn304His
NM_001312692.1:c.664A>C	NP_001299621.1:p.Asn222His
NM_017646.4:c.910A>C	NP_060116.2:p.Asn304His
NM_017646.5:c.910A>C	NP_060116.2:p.Asn304His
NR_132401.1:n.926A>C
NR_132402.1:n.784A>C
NR_132403.1:n.780A>C
NR_132404.1:n.780A>C
NR_132405.1:n.776A>C
NR_132406.1:n.686-269A>C
NR_132407.1:n.544A>C
NR_132408.1:n.540A>C
NR_132409.1:n.401A>C
NR_132410.1:n.446-269A>C
NR_132412.1:n.307-269A>C
NR_132413.1:n.195-2926A>C
NR_132414.1:n.195-5653A>C
NR_132415.1:n.1017A>C
XM_005270954.1:c.667A>C	XP_005271011.1:p.Asn223His
XM_006710706.1:c.487A>C	XP_006710769.1:p.Asn163His
XM_005270954.2:c.667A>C	XP_005271011.1:p.Asn223His
XR_946672.2:n.1010A>C
NM_017646.6:c.910A>C MANE Select	NP_060116.2:p.Asn304His