Canonical Allele Identifier: CA413607828

Gene: TEX11

Linked Data

• MyVariant Identifiers: chrX:g.70072927A>T (hg19) ; chrX:g.70853077A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70853077A>T , CM000685.2:g.70853077A>T	GRCh38
NC_000023.10:g.70072927A>T , CM000685.1:g.70072927A>T	GRCh37
NC_000023.9:g.69989652A>T	NCBI36
NG_012574.1:g.60641T>A
NG_012574.2:g.60641T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374333.7:c.482T>A MANE Select	ENSP00000363453.2:p.Val161Asp
ENST00000344304.3:c.527T>A	ENSP00000340995.3:p.Val176Asp
ENST00000374333.6:c.482T>A	ENSP00000363453.2:p.Val161Asp
ENST00000395889.6:c.527T>A	ENSP00000379226.2:p.Val176Asp
NM_001003811.1:c.527T>A	NP_001003811.1:p.Val176Asp
NM_031276.2:c.482T>A	NP_112566.2:p.Val161Asp
XM_011530994.1:c.482T>A	XP_011529296.1:p.Val161Asp
XM_017029649.1:c.482T>A	XP_016885138.1:p.Val161Asp
NM_001003811.2:c.527T>A	NP_001003811.1:p.Val176Asp
NM_031276.3:c.482T>A MANE Select	NP_112566.2:p.Val161Asp