Canonical Allele Identifier: CA2616301416

Gene: TREH

Linked Data

• gnomAD v4: 11-118663285-CCTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118663289_118663291del , CM000673.2:g.118663289_118663291del	GRCh38
NC_000011.9:g.118533998_118534000del , CM000673.1:g.118533998_118534000del	GRCh37
NC_000011.8:g.118039208_118039210del	NCBI36
NG_023321.1:g.21385_21387del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264029.9:c.190+51_190+53del MANE Select	ENSP00000264029.5:n.190+51_190+53del
ENST00000264029.8:c.190+51_190+53del	ENSP00000264029.5:n.190+51_190+53del
ENST00000397925.2:c.190+51_190+53del	ENSP00000381020.2:n.190+51_190+53del
ENST00000527558.1:n.153-92_153-90del
ENST00000531295.5:n.209+51_209+53del
ENST00000613915.4:c.90-92_90-90del	ENSP00000477923.1:n.90-92_90-90del
NM_001301065.1:c.190+51_190+53del	NP_001287994.1:n.190+51_190+53del
NM_007180.2:c.190+51_190+53del	NP_009111.2:n.190+51_190+53del
XM_011542564.1:c.-233-92_-233-90del	XP_011540866.1:n.-233-92_-233-90del
NM_001301065.2:c.190+51_190+53del	NP_001287994.1:n.190+51_190+53del
NM_007180.3:c.190+51_190+53del MANE Select	NP_009111.2:n.190+51_190+53del