Canonical Allele Identifier: CA2003585677
Gene: TREH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118659657G= , CM000673.2:g.118659657G= GRCh38
NC_000011.9:g.118530366G= , CM000673.1:g.118530366G= GRCh37
NC_000011.8:g.118035576G= NCBI36
NG_023321.1:g.25016C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264029.9:c.1320+90C= MANE Select ENSP00000264029.5:n.1320+90C=
ENST00000264029.8:c.1320+90C= ENSP00000264029.5:n.1320+90C=
ENST00000397925.2:c.1227+90C= ENSP00000381020.2:n.1227+90C=
ENST00000613915.4:c.*1097+90C= ENSP00000477923.1:n.*1097+90C=
NM_001301065.1:c.1227+90C= NP_001287994.1:n.1227+90C=
NM_007180.2:c.1320+90C= NP_009111.2:n.1320+90C=
XM_011542564.1:c.897+90C= XP_011540866.1:n.897+90C=
NM_001301065.2:c.1227+90C= NP_001287994.1:n.1227+90C=
NM_007180.3:c.1320+90C= MANE Select NP_009111.2:n.1320+90C=