Canonical Allele Identifier: CA516760234

Gene: TEX11

Linked Data

• MyVariant Identifiers: chrX:g.70073143A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70853293A>T , CM000685.2:g.70853293A>T	GRCh38
NC_000023.10:g.70073143A>T , CM000685.1:g.70073143A>T	GRCh37
NC_000023.9:g.69989868A>T	NCBI36
NG_012574.1:g.60425T>A
NG_012574.2:g.60425T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374333.7:c.360T>A MANE Select	ENSP00000363453.2:p.Ala120=
ENST00000344304.3:c.405T>A	ENSP00000340995.3:p.Ala135=
ENST00000374333.6:c.360T>A	ENSP00000363453.2:p.Ala120=
ENST00000395889.6:c.405T>A	ENSP00000379226.2:p.Ala135=
NM_001003811.1:c.405T>A	NP_001003811.1:p.Ala135=
NM_031276.2:c.360T>A	NP_112566.2:p.Ala120=
XM_011530994.1:c.360T>A	XP_011529296.1:p.Ala120=
XM_017029649.1:c.360T>A	XP_016885138.1:p.Ala120=
NM_001003811.2:c.405T>A	NP_001003811.1:p.Ala135=
NM_031276.3:c.360T>A MANE Select	NP_112566.2:p.Ala120=