Canonical Allele Identifier: CA413608177

Gene: TEX11

Linked Data

• dbSNP Id: rs1290827505
• MyVariant Identifiers: chrX:g.70073169T>C (hg19) ; chrX:g.70853319T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70853319T>C , CM000685.2:g.70853319T>C	GRCh38
NC_000023.10:g.70073169T>C , CM000685.1:g.70073169T>C	GRCh37
NC_000023.9:g.69989894T>C	NCBI36
NG_012574.1:g.60399A>G
NG_012574.2:g.60399A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374333.7:c.334A>G MANE Select	ENSP00000363453.2:p.Arg112Gly
ENST00000344304.3:c.379A>G	ENSP00000340995.3:p.Arg127Gly
ENST00000374333.6:c.334A>G	ENSP00000363453.2:p.Arg112Gly
ENST00000395889.6:c.379A>G	ENSP00000379226.2:p.Arg127Gly
NM_001003811.1:c.379A>G	NP_001003811.1:p.Arg127Gly
NM_031276.2:c.334A>G	NP_112566.2:p.Arg112Gly
XM_011530994.1:c.334A>G	XP_011529296.1:p.Arg112Gly
XM_017029649.1:c.334A>G	XP_016885138.1:p.Arg112Gly
NM_001003811.2:c.379A>G	NP_001003811.1:p.Arg127Gly
NM_031276.3:c.334A>G MANE Select	NP_112566.2:p.Arg112Gly