Canonical Allele Identifier: CA2436261269
Gene: TEX11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.70853253C= , CM000685.2:g.70853253C= GRCh38
NC_000023.10:g.70073103C= , CM000685.1:g.70073103C= GRCh37
NC_000023.9:g.69989828C= NCBI36
NG_012574.1:g.60465G=
NG_012574.2:g.60465G=

Transcript Alleles

HGVS Amino-acid change
ENST00000374333.7:c.400G= MANE Select ENSP00000363453.2:p.Val134=
ENST00000344304.3:c.445G= ENSP00000340995.3:p.Val149=
ENST00000374333.6:c.400G= ENSP00000363453.2:p.Val134=
ENST00000395889.6:c.445G= ENSP00000379226.2:p.Val149=
NM_001003811.1:c.445G= NP_001003811.1:p.Val149=
NM_031276.2:c.400G= NP_112566.2:p.Val134=
XM_011530994.1:c.400G= XP_011529296.1:p.Val134=
XM_017029649.1:c.400G= XP_016885138.1:p.Val134=
NM_001003811.2:c.445G= NP_001003811.1:p.Val149=
NM_031276.3:c.400G= MANE Select NP_112566.2:p.Val134=