Canonical Allele Identifier: CA2616301761
Gene: TREH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118663402_118663412del , CM000673.2:g.118663402_118663412del GRCh38
NC_000011.9:g.118534111_118534121del , CM000673.1:g.118534111_118534121del GRCh37
NC_000011.8:g.118039321_118039331del NCBI36
NG_023321.1:g.21264_21274del

Transcript Alleles

HGVS Amino-acid Change
ENST00000264029.9:c.120_130del MANE Select ENSP00000264029.5:p.Gln41GlyfsTer7
ENST00000264029.8:c.120_130del ENSP00000264029.5:p.Gln41GlyfsTer7
ENST00000397925.2:c.120_130del ENSP00000381020.2:p.Gln41GlyfsTer7
ENST00000527558.1:n.153-213_153-203del
ENST00000531295.5:n.139_149del
ENST00000613915.4:c.90-213_90-203del ENSP00000477923.1:n.90-213_90-203del
NM_001301065.1:c.120_130del NP_001287994.1:p.Gln41GlyfsTer7
NM_007180.2:c.120_130del NP_009111.2:p.Gln41GlyfsTer7
XM_011542564.1:c.-233-213_-233-203del XP_011540866.1:n.-233-213_-233-203del
NM_001301065.2:c.120_130del NP_001287994.1:p.Gln41GlyfsTer7
NM_007180.3:c.120_130del MANE Select NP_009111.2:p.Gln41GlyfsTer7