Canonical Allele Identifier: CA2003585687

Gene: TREH

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118659669_118659670delinsTC , CM000673.2:g.118659669_118659670delinsTC	GRCh38
NC_000011.9:g.118530378_118530379delinsTC , CM000673.1:g.118530378_118530379delinsTC	GRCh37
NC_000011.8:g.118035588_118035589delinsTC	NCBI36
NG_023321.1:g.25003_25004delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264029.9:c.1320+77_1320+78delinsGA MANE Select	ENSP00000264029.5:n.1320+77_1320+78delinsGA
ENST00000264029.8:c.1320+77_1320+78delinsGA	ENSP00000264029.5:n.1320+77_1320+78delinsGA
ENST00000397925.2:c.1227+77_1227+78delinsGA	ENSP00000381020.2:n.1227+77_1227+78delinsGA
ENST00000613915.4:c.*1097+77_*1097+78delinsGA	ENSP00000477923.1:n.*1097+77_*1097+78delinsGA
NM_001301065.1:c.1227+77_1227+78delinsGA	NP_001287994.1:n.1227+77_1227+78delinsGA
NM_007180.2:c.1320+77_1320+78delinsGA	NP_009111.2:n.1320+77_1320+78delinsGA
XM_011542564.1:c.897+77_897+78delinsGA	XP_011540866.1:n.897+77_897+78delinsGA
NM_001301065.2:c.1227+77_1227+78delinsGA	NP_001287994.1:n.1227+77_1227+78delinsGA
NM_007180.3:c.1320+77_1320+78delinsGA MANE Select	NP_009111.2:n.1320+77_1320+78delinsGA