Canonical Allele Identifier: CA2616304966

Gene: TREH

Linked Data

• gnomAD v4: 11-118659644-AGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118659647_118659648del , CM000673.2:g.118659647_118659648del	GRCh38
NC_000011.9:g.118530356_118530357del , CM000673.1:g.118530356_118530357del	GRCh37
NC_000011.8:g.118035566_118035567del	NCBI36
NG_023321.1:g.25027_25028del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264029.9:c.1320+101_1320+102del MANE Select	ENSP00000264029.5:n.1320+101_1320+102del
ENST00000264029.8:c.1320+101_1320+102del	ENSP00000264029.5:n.1320+101_1320+102del
ENST00000397925.2:c.1227+101_1227+102del	ENSP00000381020.2:n.1227+101_1227+102del
ENST00000613915.4:c.*1097+101_*1097+102del	ENSP00000477923.1:n.*1097+101_*1097+102del
NM_001301065.1:c.1227+101_1227+102del	NP_001287994.1:n.1227+101_1227+102del
NM_007180.2:c.1320+101_1320+102del	NP_009111.2:n.1320+101_1320+102del
XM_011542564.1:c.897+101_897+102del	XP_011540866.1:n.897+101_897+102del
NM_001301065.2:c.1227+101_1227+102del	NP_001287994.1:n.1227+101_1227+102del
NM_007180.3:c.1320+101_1320+102del MANE Select	NP_009111.2:n.1320+101_1320+102del