Canonical Allele Identifier: CA2003593287
Gene: TREH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118663298G= , CM000673.2:g.118663298G= GRCh38
NC_000011.9:g.118534007G= , CM000673.1:g.118534007G= GRCh37
NC_000011.8:g.118039217G= NCBI36
NG_023321.1:g.21375C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264029.9:c.190+41C= MANE Select ENSP00000264029.5:n.190+41C=
ENST00000264029.8:c.190+41C= ENSP00000264029.5:n.190+41C=
ENST00000397925.2:c.190+41C= ENSP00000381020.2:n.190+41C=
ENST00000527558.1:n.153-102C=
ENST00000531295.5:n.209+41C=
ENST00000613915.4:c.90-102C= ENSP00000477923.1:n.90-102C=
NM_001301065.1:c.190+41C= NP_001287994.1:n.190+41C=
NM_007180.2:c.190+41C= NP_009111.2:n.190+41C=
XM_011542564.1:c.-233-102C= XP_011540866.1:n.-233-102C=
NM_001301065.2:c.190+41C= NP_001287994.1:n.190+41C=
NM_007180.3:c.190+41C= MANE Select NP_009111.2:n.190+41C=