Canonical Allele Identifier: CA413608164
Gene: TEX11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.70853313C>G , CM000685.2:g.70853313C>G GRCh38
NC_000023.10:g.70073163C>G , CM000685.1:g.70073163C>G GRCh37
NC_000023.9:g.69989888C>G NCBI36
NG_012574.1:g.60405G>C
NG_012574.2:g.60405G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000374333.7:c.340G>C MANE Select ENSP00000363453.2:p.Gly114Arg
ENST00000344304.3:c.385G>C ENSP00000340995.3:p.Gly129Arg
ENST00000374333.6:c.340G>C ENSP00000363453.2:p.Gly114Arg
ENST00000395889.6:c.385G>C ENSP00000379226.2:p.Gly129Arg
NM_001003811.1:c.385G>C NP_001003811.1:p.Gly129Arg
NM_031276.2:c.340G>C NP_112566.2:p.Gly114Arg
XM_011530994.1:c.340G>C XP_011529296.1:p.Gly114Arg
XM_017029649.1:c.340G>C XP_016885138.1:p.Gly114Arg
NM_001003811.2:c.385G>C NP_001003811.1:p.Gly129Arg
NM_031276.3:c.340G>C MANE Select NP_112566.2:p.Gly114Arg