Canonical Allele Identifier: CA672369130

Gene: TREH

Linked Data

• dbSNP Id: rs1218845266
• gnomAD v3: 11-118659661-A-G
• gnomAD v4: 11-118659661-A-G
• MyVariant Identifiers: chr11:g.118659661A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118659661A>G , CM000673.2:g.118659661A>G	GRCh38
NC_000011.9:g.118530370A>G , CM000673.1:g.118530370A>G	GRCh37
NC_000011.8:g.118035580A>G	NCBI36
NG_023321.1:g.25012T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264029.9:c.1320+86T>C MANE Select	ENSP00000264029.5:n.1320+86T>C
ENST00000264029.8:c.1320+86T>C	ENSP00000264029.5:n.1320+86T>C
ENST00000397925.2:c.1227+86T>C	ENSP00000381020.2:n.1227+86T>C
ENST00000613915.4:c.*1097+86T>C	ENSP00000477923.1:n.*1097+86T>C
NM_001301065.1:c.1227+86T>C	NP_001287994.1:n.1227+86T>C
NM_007180.2:c.1320+86T>C	NP_009111.2:n.1320+86T>C
XM_011542564.1:c.897+86T>C	XP_011540866.1:n.897+86T>C
NM_001301065.2:c.1227+86T>C	NP_001287994.1:n.1227+86T>C
NM_007180.3:c.1320+86T>C MANE Select	NP_009111.2:n.1320+86T>C