Canonical Allele Identifier: CA339832744

Gene: TRIT1

Linked Data

• MyVariant Identifiers: chr1:g.40312933G>C (hg19) ; chr1:g.39847261G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.39847261G>C , CM000663.2:g.39847261G>C	GRCh38
NC_000001.10:g.40312933G>C , CM000663.1:g.40312933G>C	GRCh37
NC_000001.9:g.40085520G>C	NCBI36
NG_042822.1:g.41251C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000316891.10:c.965C>G MANE Select	ENSP00000321810.5:p.Ala322Gly
ENST00000648678.1:c.1857C>G	ENSP00000497805.1:n.1857C>G
ENST00000316891.9:c.965C>G	ENSP00000321810.5:p.Ala322Gly
ENST00000372818.5:c.928+287C>G	ENSP00000361905.1:n.928+287C>G
ENST00000441669.6:c.719C>G	ENSP00000388333.2:p.Ala240Gly
ENST00000462797.5:c.965C>G	ENSP00000473773.1:p.Ala322Gly
ENST00000465417.5:n.149C>G
ENST00000467774.1:n.247C>G
ENST00000489945.5:c.*383C>G	ENSP00000473745.1:n.*383C>G
ENST00000491865.5:n.200C>G
ENST00000492612.6:c.809C>G
ENST00000495175.6:c.*387C>G	ENSP00000474264.1:n.*387C>G
ENST00000537440.5:c.53C>G	ENSP00000437700.1:p.Ala18Gly
ENST00000541099.5:c.-140-2621C>G	ENSP00000437896.1:n.-140-2621C>G
NM_001312691.1:c.928+287C>G	NP_001299620.1:n.928+287C>G
NM_001312692.1:c.719C>G	NP_001299621.1:p.Ala240Gly
NM_017646.4:c.965C>G	NP_060116.2:p.Ala322Gly
NM_017646.5:c.965C>G	NP_060116.2:p.Ala322Gly
NR_132401.1:n.981C>G
NR_132402.1:n.839C>G
NR_132403.1:n.835C>G
NR_132404.1:n.835C>G
NR_132405.1:n.831C>G
NR_132406.1:n.722C>G
NR_132407.1:n.599C>G
NR_132408.1:n.595C>G
NR_132409.1:n.456C>G
NR_132410.1:n.482C>G
NR_132412.1:n.343C>G
NR_132413.1:n.195-2621C>G
NR_132414.1:n.195-5348C>G
NR_132415.1:n.1072C>G
XM_005270954.1:c.722C>G	XP_005271011.1:p.Ala241Gly
XM_006710706.1:c.542C>G	XP_006710769.1:p.Ala181Gly
XM_005270954.2:c.722C>G	XP_005271011.1:p.Ala241Gly
XR_946672.2:n.1065C>G
NM_017646.6:c.965C>G MANE Select	NP_060116.2:p.Ala322Gly