Canonical Allele Identifier: CA516760412
Gene: TEX11 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.70073167T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.70853317T>C , CM000685.2:g.70853317T>C GRCh38
NC_000023.10:g.70073167T>C , CM000685.1:g.70073167T>C GRCh37
NC_000023.9:g.69989892T>C NCBI36
NG_012574.1:g.60401A>G
NG_012574.2:g.60401A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000374333.7:c.336A>G MANE Select ENSP00000363453.2:p.Arg112=
ENST00000344304.3:c.381A>G ENSP00000340995.3:p.Arg127=
ENST00000374333.6:c.336A>G ENSP00000363453.2:p.Arg112=
ENST00000395889.6:c.381A>G ENSP00000379226.2:p.Arg127=
NM_001003811.1:c.381A>G NP_001003811.1:p.Arg127=
NM_031276.2:c.336A>G NP_112566.2:p.Arg112=
XM_011530994.1:c.336A>G XP_011529296.1:p.Arg112=
XM_017029649.1:c.336A>G XP_016885138.1:p.Arg112=
NM_001003811.2:c.381A>G NP_001003811.1:p.Arg127=
NM_031276.3:c.336A>G MANE Select NP_112566.2:p.Arg112=