Canonical Allele Identifier: CA2003585707

Gene: TREH

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118659688_118659689delinsAG , CM000673.2:g.118659688_118659689delinsAG	GRCh38
NC_000011.9:g.118530397_118530398delinsAG , CM000673.1:g.118530397_118530398delinsAG	GRCh37
NC_000011.8:g.118035607_118035608delinsAG	NCBI36
NG_023321.1:g.24984_24985delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264029.9:c.1320+58_1320+59delinsCT MANE Select	ENSP00000264029.5:n.1320+58_1320+59delinsCT
ENST00000264029.8:c.1320+58_1320+59delinsCT	ENSP00000264029.5:n.1320+58_1320+59delinsCT
ENST00000397925.2:c.1227+58_1227+59delinsCT	ENSP00000381020.2:n.1227+58_1227+59delinsCT
ENST00000613915.4:c.*1097+58_*1097+59delinsCT	ENSP00000477923.1:n.*1097+58_*1097+59delinsCT
NM_001301065.1:c.1227+58_1227+59delinsCT	NP_001287994.1:n.1227+58_1227+59delinsCT
NM_007180.2:c.1320+58_1320+59delinsCT	NP_009111.2:n.1320+58_1320+59delinsCT
XM_011542564.1:c.897+58_897+59delinsCT	XP_011540866.1:n.897+58_897+59delinsCT
NM_001301065.2:c.1227+58_1227+59delinsCT	NP_001287994.1:n.1227+58_1227+59delinsCT
NM_007180.3:c.1320+58_1320+59delinsCT MANE Select	NP_009111.2:n.1320+58_1320+59delinsCT