Canonical Allele Identifier: CA2436261286
Gene: TEX11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.70853319T= , CM000685.2:g.70853319T= GRCh38
NC_000023.10:g.70073169T= , CM000685.1:g.70073169T= GRCh37
NC_000023.9:g.69989894T= NCBI36
NG_012574.1:g.60399A=
NG_012574.2:g.60399A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374333.7:c.334A= MANE Select ENSP00000363453.2:p.Arg112=
ENST00000344304.3:c.379A= ENSP00000340995.3:p.Arg127=
ENST00000374333.6:c.334A= ENSP00000363453.2:p.Arg112=
ENST00000395889.6:c.379A= ENSP00000379226.2:p.Arg127=
NM_001003811.1:c.379A= NP_001003811.1:p.Arg127=
NM_031276.2:c.334A= NP_112566.2:p.Arg112=
XM_011530994.1:c.334A= XP_011529296.1:p.Arg112=
XM_017029649.1:c.334A= XP_016885138.1:p.Arg112=
NM_001003811.2:c.379A= NP_001003811.1:p.Arg127=
NM_031276.3:c.334A= MANE Select NP_112566.2:p.Arg112=