Canonical Allele Identifier: CA2793820244
Gene: TREH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118663321del , CM000673.2:g.118663321del GRCh38
NC_000011.9:g.118534030del , CM000673.1:g.118534030del GRCh37
NC_000011.8:g.118039240del NCBI36
NG_023321.1:g.21352del

Transcript Alleles

HGVS Amino-acid Change
ENST00000264029.9:c.190+18del MANE Select ENSP00000264029.5:n.190+18del
ENST00000264029.8:c.190+18del ENSP00000264029.5:n.190+18del
ENST00000397925.2:c.190+18del ENSP00000381020.2:n.190+18del
ENST00000527558.1:n.153-125del
ENST00000531295.5:n.209+18del
ENST00000613915.4:c.90-125del ENSP00000477923.1:n.90-125del
NM_001301065.1:c.190+18del NP_001287994.1:n.190+18del
NM_007180.2:c.190+18del NP_009111.2:n.190+18del
XM_011542564.1:c.-233-125del XP_011540866.1:n.-233-125del
NM_001301065.2:c.190+18del NP_001287994.1:n.190+18del
NM_007180.3:c.190+18del MANE Select NP_009111.2:n.190+18del