Canonical Allele Identifier: CA2579637150
Gene: TEX11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.70853363dup , CM000685.2:g.70853363dup GRCh38
NC_000023.10:g.70073213dup , CM000685.1:g.70073213dup GRCh37
NC_000023.9:g.69989938dup NCBI36
NG_012574.1:g.60359dup
NG_012574.2:g.60359dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000374333.7:c.325-31dup MANE Select ENSP00000363453.2:n.325-31dup
ENST00000344304.3:c.370-31dup ENSP00000340995.3:n.370-31dup
ENST00000374333.6:c.325-31dup ENSP00000363453.2:n.325-31dup
ENST00000395889.6:c.370-31dup ENSP00000379226.2:n.370-31dup
NM_001003811.1:c.370-31dup NP_001003811.1:n.370-31dup
NM_031276.2:c.325-31dup NP_112566.2:n.325-31dup
XM_011530994.1:c.325-31dup XP_011529296.1:n.325-31dup
XM_017029649.1:c.325-31dup XP_016885138.1:n.325-31dup
NM_001003811.2:c.370-31dup NP_001003811.1:n.370-31dup
NM_031276.3:c.325-31dup MANE Select NP_112566.2:n.325-31dup