Canonical Allele Identifier: CA413608122
Gene: TEX11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.70853296A>T , CM000685.2:g.70853296A>T GRCh38
NC_000023.10:g.70073146A>T , CM000685.1:g.70073146A>T GRCh37
NC_000023.9:g.69989871A>T NCBI36
NG_012574.1:g.60422T>A
NG_012574.2:g.60422T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000374333.7:c.357T>A MANE Select ENSP00000363453.2:p.Asp119Glu
ENST00000344304.3:c.402T>A ENSP00000340995.3:p.Asp134Glu
ENST00000374333.6:c.357T>A ENSP00000363453.2:p.Asp119Glu
ENST00000395889.6:c.402T>A ENSP00000379226.2:p.Asp134Glu
NM_001003811.1:c.402T>A NP_001003811.1:p.Asp134Glu
NM_031276.2:c.357T>A NP_112566.2:p.Asp119Glu
XM_011530994.1:c.357T>A XP_011529296.1:p.Asp119Glu
XM_017029649.1:c.357T>A XP_016885138.1:p.Asp119Glu
NM_001003811.2:c.402T>A NP_001003811.1:p.Asp134Glu
NM_031276.3:c.357T>A MANE Select NP_112566.2:p.Asp119Glu