Canonical Allele Identifier: CA2436261233
Gene: TEX11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.70853135C= , CM000685.2:g.70853135C= GRCh38
NC_000023.10:g.70072985C= , CM000685.1:g.70072985C= GRCh37
NC_000023.9:g.69989710C= NCBI36
NG_012574.1:g.60583G=
NG_012574.2:g.60583G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374333.7:c.424G= MANE Select ENSP00000363453.2:p.Val142=
ENST00000344304.3:c.469G= ENSP00000340995.3:p.Val157=
ENST00000374333.6:c.424G= ENSP00000363453.2:p.Val142=
ENST00000395889.6:c.469G= ENSP00000379226.2:p.Val157=
NM_001003811.1:c.469G= NP_001003811.1:p.Val157=
NM_031276.2:c.424G= NP_112566.2:p.Val142=
XM_011530994.1:c.424G= XP_011529296.1:p.Val142=
XM_017029649.1:c.424G= XP_016885138.1:p.Val142=
NM_001003811.2:c.469G= NP_001003811.1:p.Val157=
NM_031276.3:c.424G= MANE Select NP_112566.2:p.Val142=