Canonical Allele Identifier: CA2436261230
Gene: TEX11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.70853126T= , CM000685.2:g.70853126T= GRCh38
NC_000023.10:g.70072976T= , CM000685.1:g.70072976T= GRCh37
NC_000023.9:g.69989701T= NCBI36
NG_012574.1:g.60592A=
NG_012574.2:g.60592A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374333.7:c.433A= MANE Select ENSP00000363453.2:p.Ile145=
ENST00000344304.3:c.478A= ENSP00000340995.3:p.Ile160=
ENST00000374333.6:c.433A= ENSP00000363453.2:p.Ile145=
ENST00000395889.6:c.478A= ENSP00000379226.2:p.Ile160=
NM_001003811.1:c.478A= NP_001003811.1:p.Ile160=
NM_031276.2:c.433A= NP_112566.2:p.Ile145=
XM_011530994.1:c.433A= XP_011529296.1:p.Ile145=
XM_017029649.1:c.433A= XP_016885138.1:p.Ile145=
NM_001003811.2:c.478A= NP_001003811.1:p.Ile160=
NM_031276.3:c.433A= MANE Select NP_112566.2:p.Ile145=