Canonical Allele Identifier: CA413608064
Gene: TEX11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.70853269T>G , CM000685.2:g.70853269T>G GRCh38
NC_000023.10:g.70073119T>G , CM000685.1:g.70073119T>G GRCh37
NC_000023.9:g.69989844T>G NCBI36
NG_012574.1:g.60449A>C
NG_012574.2:g.60449A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000374333.7:c.384A>C MANE Select ENSP00000363453.2:p.Glu128Asp
ENST00000344304.3:c.429A>C ENSP00000340995.3:p.Glu143Asp
ENST00000374333.6:c.384A>C ENSP00000363453.2:p.Glu128Asp
ENST00000395889.6:c.429A>C ENSP00000379226.2:p.Glu143Asp
NM_001003811.1:c.429A>C NP_001003811.1:p.Glu143Asp
NM_031276.2:c.384A>C NP_112566.2:p.Glu128Asp
XM_011530994.1:c.384A>C XP_011529296.1:p.Glu128Asp
XM_017029649.1:c.384A>C XP_016885138.1:p.Glu128Asp
NM_001003811.2:c.429A>C NP_001003811.1:p.Glu143Asp
NM_031276.3:c.384A>C MANE Select NP_112566.2:p.Glu128Asp