Canonical Allele Identifier: CA413608150

Gene: TEX11

Linked Data

• COSMIC: COSM3973817 ; COSM4908718
• MyVariant Identifiers: chrX:g.70073157C>A (hg19) ; chrX:g.70853307C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70853307C>A , CM000685.2:g.70853307C>A	GRCh38
NC_000023.10:g.70073157C>A , CM000685.1:g.70073157C>A	GRCh37
NC_000023.9:g.69989882C>A	NCBI36
NG_012574.1:g.60411G>T
NG_012574.2:g.60411G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374333.7:c.346G>T MANE Select	ENSP00000363453.2:p.Glu116Ter
ENST00000344304.3:c.391G>T	ENSP00000340995.3:p.Glu131Ter
ENST00000374333.6:c.346G>T	ENSP00000363453.2:p.Glu116Ter
ENST00000395889.6:c.391G>T	ENSP00000379226.2:p.Glu131Ter
NM_001003811.1:c.391G>T	NP_001003811.1:p.Glu131Ter
NM_031276.2:c.346G>T	NP_112566.2:p.Glu116Ter
XM_011530994.1:c.346G>T	XP_011529296.1:p.Glu116Ter
XM_017029649.1:c.346G>T	XP_016885138.1:p.Glu116Ter
NM_001003811.2:c.391G>T	NP_001003811.1:p.Glu131Ter
NM_031276.3:c.346G>T MANE Select	NP_112566.2:p.Glu116Ter