Canonical Allele Identifier: CA2436261232
Gene: TEX11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.70853132T= , CM000685.2:g.70853132T= GRCh38
NC_000023.10:g.70072982T= , CM000685.1:g.70072982T= GRCh37
NC_000023.9:g.69989707T= NCBI36
NG_012574.1:g.60586A=
NG_012574.2:g.60586A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374333.7:c.427A= MANE Select ENSP00000363453.2:p.Lys143=
ENST00000344304.3:c.472A= ENSP00000340995.3:p.Lys158=
ENST00000374333.6:c.427A= ENSP00000363453.2:p.Lys143=
ENST00000395889.6:c.472A= ENSP00000379226.2:p.Lys158=
NM_001003811.1:c.472A= NP_001003811.1:p.Lys158=
NM_031276.2:c.427A= NP_112566.2:p.Lys143=
XM_011530994.1:c.427A= XP_011529296.1:p.Lys143=
XM_017029649.1:c.427A= XP_016885138.1:p.Lys143=
NM_001003811.2:c.472A= NP_001003811.1:p.Lys158=
NM_031276.3:c.427A= MANE Select NP_112566.2:p.Lys143=