Canonical Allele Identifier: CA2579637147
Gene: TEX11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.70853261del , CM000685.2:g.70853261del GRCh38
NC_000023.10:g.70073111del , CM000685.1:g.70073111del GRCh37
NC_000023.9:g.69989836del NCBI36
NG_012574.1:g.60458del
NG_012574.2:g.60458del

Transcript Alleles

HGVS Amino-acid change
ENST00000374333.7:c.393del MANE Select ENSP00000363453.2:p.Ala132LeufsTer13
ENST00000344304.3:c.438del ENSP00000340995.3:p.Ala147LeufsTer13
ENST00000374333.6:c.393del ENSP00000363453.2:p.Ala132LeufsTer13
ENST00000395889.6:c.438del ENSP00000379226.2:p.Ala147LeufsTer13
NM_001003811.1:c.438del NP_001003811.1:p.Ala147LeufsTer13
NM_031276.2:c.393del NP_112566.2:p.Ala132LeufsTer13
XM_011530994.1:c.393del XP_011529296.1:p.Ala132LeufsTer13
XM_017029649.1:c.393del XP_016885138.1:p.Ala132LeufsTer13
NM_001003811.2:c.438del NP_001003811.1:p.Ala147LeufsTer13
NM_031276.3:c.393del MANE Select NP_112566.2:p.Ala132LeufsTer13