Canonical Allele Identifier: CA672369141

Gene: TREH

Linked Data

• dbSNP Id: rs1449530418
• MyVariant Identifiers: chr11:g.118659670del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118659673del , CM000673.2:g.118659673del	GRCh38
NC_000011.9:g.118530382del , CM000673.1:g.118530382del	GRCh37
NC_000011.8:g.118035592del	NCBI36
NG_023321.1:g.25003del

Transcript Alleles

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