Canonical Allele Identifier: CA413607835

Gene: TEX11

Linked Data

• MyVariant Identifiers: chrX:g.70072931T>A (hg19) ; chrX:g.70853081T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70853081T>A , CM000685.2:g.70853081T>A	GRCh38
NC_000023.10:g.70072931T>A , CM000685.1:g.70072931T>A	GRCh37
NC_000023.9:g.69989656T>A	NCBI36
NG_012574.1:g.60637A>T
NG_012574.2:g.60637A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374333.7:c.478A>T MANE Select	ENSP00000363453.2:p.Thr160Ser
ENST00000344304.3:c.523A>T	ENSP00000340995.3:p.Thr175Ser
ENST00000374333.6:c.478A>T	ENSP00000363453.2:p.Thr160Ser
ENST00000395889.6:c.523A>T	ENSP00000379226.2:p.Thr175Ser
NM_001003811.1:c.523A>T	NP_001003811.1:p.Thr175Ser
NM_031276.2:c.478A>T	NP_112566.2:p.Thr160Ser
XM_011530994.1:c.478A>T	XP_011529296.1:p.Thr160Ser
XM_017029649.1:c.478A>T	XP_016885138.1:p.Thr160Ser
NM_001003811.2:c.523A>T	NP_001003811.1:p.Thr175Ser
NM_031276.3:c.478A>T MANE Select	NP_112566.2:p.Thr160Ser