Canonical Allele Identifier: CA2003593371
Gene: TREH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118663398A= , CM000673.2:g.118663398A= GRCh38
NC_000011.9:g.118534107A= , CM000673.1:g.118534107A= GRCh37
NC_000011.8:g.118039317A= NCBI36
NG_023321.1:g.21275T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264029.9:c.131T= MANE Select ENSP00000264029.5:p.Met44=
ENST00000264029.8:c.131T= ENSP00000264029.5:p.Met44=
ENST00000397925.2:c.131T= ENSP00000381020.2:p.Met44=
ENST00000527558.1:n.153-202T=
ENST00000531295.5:n.150T=
ENST00000613915.4:c.90-202T= ENSP00000477923.1:n.90-202T=
NM_001301065.1:c.131T= NP_001287994.1:p.Met44=
NM_007180.2:c.131T= NP_009111.2:p.Met44=
XM_011542564.1:c.-233-202T= XP_011540866.1:n.-233-202T=
NM_001301065.2:c.131T= NP_001287994.1:p.Met44=
NM_007180.3:c.131T= MANE Select NP_009111.2:p.Met44=