Canonical Allele Identifier: CA2579637148
Gene: TEX11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.70853274del , CM000685.2:g.70853274del GRCh38
NC_000023.10:g.70073124del , CM000685.1:g.70073124del GRCh37
NC_000023.9:g.69989849del NCBI36
NG_012574.1:g.60444del
NG_012574.2:g.60444del

Transcript Alleles

HGVS Amino-acid Change
ENST00000374333.7:c.379del MANE Select ENSP00000363453.2:p.Asp127MetfsTer18
ENST00000344304.3:c.424del ENSP00000340995.3:p.Asp142MetfsTer18
ENST00000374333.6:c.379del ENSP00000363453.2:p.Asp127MetfsTer18
ENST00000395889.6:c.424del ENSP00000379226.2:p.Asp142MetfsTer18
NM_001003811.1:c.424del NP_001003811.1:p.Asp142MetfsTer18
NM_031276.2:c.379del NP_112566.2:p.Asp127MetfsTer18
XM_011530994.1:c.379del XP_011529296.1:p.Asp127MetfsTer18
XM_017029649.1:c.379del XP_016885138.1:p.Asp127MetfsTer18
NM_001003811.2:c.424del NP_001003811.1:p.Asp142MetfsTer18
NM_031276.3:c.379del MANE Select NP_112566.2:p.Asp127MetfsTer18