Canonical Allele Identifier: CA413608036

Gene: TEX11

Linked Data

• MyVariant Identifiers: chrX:g.70073108G>T (hg19) ; chrX:g.70853258G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70853258G>T , CM000685.2:g.70853258G>T	GRCh38
NC_000023.10:g.70073108G>T , CM000685.1:g.70073108G>T	GRCh37
NC_000023.9:g.69989833G>T	NCBI36
NG_012574.1:g.60460C>A
NG_012574.2:g.60460C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374333.7:c.395C>A MANE Select	ENSP00000363453.2:p.Ala132Asp
ENST00000344304.3:c.440C>A	ENSP00000340995.3:p.Ala147Asp
ENST00000374333.6:c.395C>A	ENSP00000363453.2:p.Ala132Asp
ENST00000395889.6:c.440C>A	ENSP00000379226.2:p.Ala147Asp
NM_001003811.1:c.440C>A	NP_001003811.1:p.Ala147Asp
NM_031276.2:c.395C>A	NP_112566.2:p.Ala132Asp
XM_011530994.1:c.395C>A	XP_011529296.1:p.Ala132Asp
XM_017029649.1:c.395C>A	XP_016885138.1:p.Ala132Asp
NM_001003811.2:c.440C>A	NP_001003811.1:p.Ala147Asp
NM_031276.3:c.395C>A MANE Select	NP_112566.2:p.Ala132Asp