Canonical Allele Identifier: CA2003585663

Gene: TREH

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118659646G= , CM000673.2:g.118659646G=	GRCh38
NC_000011.9:g.118530355G= , CM000673.1:g.118530355G=	GRCh37
NC_000011.8:g.118035565G=	NCBI36
NG_023321.1:g.25027C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264029.9:c.1320+101C= MANE Select	ENSP00000264029.5:n.1320+101C=
ENST00000264029.8:c.1320+101C=	ENSP00000264029.5:n.1320+101C=
ENST00000397925.2:c.1227+101C=	ENSP00000381020.2:n.1227+101C=
ENST00000613915.4:c.*1097+101C=	ENSP00000477923.1:n.*1097+101C=
NM_001301065.1:c.1227+101C=	NP_001287994.1:n.1227+101C=
NM_007180.2:c.1320+101C=	NP_009111.2:n.1320+101C=
XM_011542564.1:c.897+101C=	XP_011540866.1:n.897+101C=
NM_001301065.2:c.1227+101C=	NP_001287994.1:n.1227+101C=
NM_007180.3:c.1320+101C= MANE Select	NP_009111.2:n.1320+101C=