Canonical Allele Identifier: CA413608183

Gene: TEX11

Linked Data

• gnomAD v4: X-70853321-A-G
• MyVariant Identifiers: chrX:g.70073171A>G (hg19) ; chrX:g.70853321A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70853321A>G , CM000685.2:g.70853321A>G	GRCh38
NC_000023.10:g.70073171A>G , CM000685.1:g.70073171A>G	GRCh37
NC_000023.9:g.69989896A>G	NCBI36
NG_012574.1:g.60397T>C
NG_012574.2:g.60397T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374333.7:c.332T>C MANE Select	ENSP00000363453.2:p.Met111Thr
ENST00000344304.3:c.377T>C	ENSP00000340995.3:p.Met126Thr
ENST00000374333.6:c.332T>C	ENSP00000363453.2:p.Met111Thr
ENST00000395889.6:c.377T>C	ENSP00000379226.2:p.Met126Thr
NM_001003811.1:c.377T>C	NP_001003811.1:p.Met126Thr
NM_031276.2:c.332T>C	NP_112566.2:p.Met111Thr
XM_011530994.1:c.332T>C	XP_011529296.1:p.Met111Thr
XM_017029649.1:c.332T>C	XP_016885138.1:p.Met111Thr
NM_001003811.2:c.377T>C	NP_001003811.1:p.Met126Thr
NM_031276.3:c.332T>C MANE Select	NP_112566.2:p.Met111Thr