Canonical Allele Identifier: CA516759972

Gene: TEX11

Linked Data

• MyVariant Identifiers: chrX:g.70073110T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70853260T>C , CM000685.2:g.70853260T>C	GRCh38
NC_000023.10:g.70073110T>C , CM000685.1:g.70073110T>C	GRCh37
NC_000023.9:g.69989835T>C	NCBI36
NG_012574.1:g.60458A>G
NG_012574.2:g.60458A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000374333.7:c.393A>G MANE Select	ENSP00000363453.2:p.Gln131=
ENST00000344304.3:c.438A>G	ENSP00000340995.3:p.Gln146=
ENST00000374333.6:c.393A>G	ENSP00000363453.2:p.Gln131=
ENST00000395889.6:c.438A>G	ENSP00000379226.2:p.Gln146=
NM_001003811.1:c.438A>G	NP_001003811.1:p.Gln146=
NM_031276.2:c.393A>G	NP_112566.2:p.Gln131=
XM_011530994.1:c.393A>G	XP_011529296.1:p.Gln131=
XM_017029649.1:c.393A>G	XP_016885138.1:p.Gln131=
NM_001003811.2:c.438A>G	NP_001003811.1:p.Gln146=
NM_031276.3:c.393A>G MANE Select	NP_112566.2:p.Gln131=