Canonical Allele Identifier: CA2436261237
Gene: TEX11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.70853142T= , CM000685.2:g.70853142T= GRCh38
NC_000023.10:g.70072992T= , CM000685.1:g.70072992T= GRCh37
NC_000023.9:g.69989717T= NCBI36
NG_012574.1:g.60576A=
NG_012574.2:g.60576A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374333.7:c.417A= MANE Select ENSP00000363453.2:p.Gln139=
ENST00000344304.3:c.462A= ENSP00000340995.3:p.Gln154=
ENST00000374333.6:c.417A= ENSP00000363453.2:p.Gln139=
ENST00000395889.6:c.462A= ENSP00000379226.2:p.Gln154=
NM_001003811.1:c.462A= NP_001003811.1:p.Gln154=
NM_031276.2:c.417A= NP_112566.2:p.Gln139=
XM_011530994.1:c.417A= XP_011529296.1:p.Gln139=
XM_017029649.1:c.417A= XP_016885138.1:p.Gln139=
NM_001003811.2:c.462A= NP_001003811.1:p.Gln154=
NM_031276.3:c.417A= MANE Select NP_112566.2:p.Gln139=