Canonical Allele Identifier: CA2003593294

Gene: TREH

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118663306T= , CM000673.2:g.118663306T=	GRCh38
NC_000011.9:g.118534015T= , CM000673.1:g.118534015T=	GRCh37
NC_000011.8:g.118039225T=	NCBI36
NG_023321.1:g.21367A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000264029.9:c.190+33A= MANE Select	ENSP00000264029.5:n.190+33A=
ENST00000264029.8:c.190+33A=	ENSP00000264029.5:n.190+33A=
ENST00000397925.2:c.190+33A=	ENSP00000381020.2:n.190+33A=
ENST00000527558.1:n.153-110A=
ENST00000531295.5:n.209+33A=
ENST00000613915.4:c.90-110A=	ENSP00000477923.1:n.90-110A=
NM_001301065.1:c.190+33A=	NP_001287994.1:n.190+33A=
NM_007180.2:c.190+33A=	NP_009111.2:n.190+33A=
XM_011542564.1:c.-233-110A=	XP_011540866.1:n.-233-110A=
NM_001301065.2:c.190+33A=	NP_001287994.1:n.190+33A=
NM_007180.3:c.190+33A= MANE Select	NP_009111.2:n.190+33A=