Canonical Allele Identifier: CA2003593350
Gene: TREH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118663373C= , CM000673.2:g.118663373C= GRCh38
NC_000011.9:g.118534082C= , CM000673.1:g.118534082C= GRCh37
NC_000011.8:g.118039292C= NCBI36
NG_023321.1:g.21300G=

Transcript Alleles

HGVS Amino-acid change
ENST00000264029.9:c.156G= MANE Select ENSP00000264029.5:p.Lys52=
ENST00000264029.8:c.156G= ENSP00000264029.5:p.Lys52=
ENST00000397925.2:c.156G= ENSP00000381020.2:p.Lys52=
ENST00000527558.1:n.153-177G=
ENST00000531295.5:n.175G=
ENST00000613915.4:c.90-177G= ENSP00000477923.1:n.90-177G=
NM_001301065.1:c.156G= NP_001287994.1:p.Lys52=
NM_007180.2:c.156G= NP_009111.2:p.Lys52=
XM_011542564.1:c.-233-177G= XP_011540866.1:n.-233-177G=
NM_001301065.2:c.156G= NP_001287994.1:p.Lys52=
NM_007180.3:c.156G= MANE Select NP_009111.2:p.Lys52=