Canonical Allele Identifier: CA516759256

Gene: TEX11

Linked Data

• MyVariant Identifiers: chrX:g.70072910T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70853060T>G , CM000685.2:g.70853060T>G	GRCh38
NC_000023.10:g.70072910T>G , CM000685.1:g.70072910T>G	GRCh37
NC_000023.9:g.69989635T>G	NCBI36
NG_012574.1:g.60658A>C
NG_012574.2:g.60658A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374333.7:c.499A>C MANE Select	ENSP00000363453.2:p.Arg167=
ENST00000344304.3:c.544A>C	ENSP00000340995.3:p.Arg182=
ENST00000374333.6:c.499A>C	ENSP00000363453.2:p.Arg167=
ENST00000395889.6:c.544A>C	ENSP00000379226.2:p.Arg182=
NM_001003811.1:c.544A>C	NP_001003811.1:p.Arg182=
NM_031276.2:c.499A>C	NP_112566.2:p.Arg167=
XM_011530994.1:c.499A>C	XP_011529296.1:p.Arg167=
XM_017029649.1:c.499A>C	XP_016885138.1:p.Arg167=
NM_001003811.2:c.544A>C	NP_001003811.1:p.Arg182=
NM_031276.3:c.499A>C MANE Select	NP_112566.2:p.Arg167=