Canonical Allele Identifier: CA10442914

Gene: TEX11

Linked Data

• dbSNP Id: rs778603655
• ExAC: X:70073104 A / G
• gnomAD v2: X-70073104-A-G
• gnomAD v3: X-70853254-A-G
• gnomAD v4: X-70853254-A-G
• MyVariant Identifiers: chrX:g.70073104A>G (hg19) ; chrX:g.70853254A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70853254A>G , CM000685.2:g.70853254A>G	GRCh38
NC_000023.10:g.70073104A>G , CM000685.1:g.70073104A>G	GRCh37
NC_000023.9:g.69989829A>G	NCBI36
NG_012574.1:g.60464T>C
NG_012574.2:g.60464T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374333.7:c.399T>C MANE Select	ENSP00000363453.2:p.Ala133=
ENST00000344304.3:c.444T>C	ENSP00000340995.3:p.Ala148=
ENST00000374333.6:c.399T>C	ENSP00000363453.2:p.Ala133=
ENST00000395889.6:c.444T>C	ENSP00000379226.2:p.Ala148=
NM_001003811.1:c.444T>C	NP_001003811.1:p.Ala148=
NM_031276.2:c.399T>C	NP_112566.2:p.Ala133=
XM_011530994.1:c.399T>C	XP_011529296.1:p.Ala133=
XM_017029649.1:c.399T>C	XP_016885138.1:p.Ala133=
NM_001003811.2:c.444T>C	NP_001003811.1:p.Ala148=
NM_031276.3:c.399T>C MANE Select	NP_112566.2:p.Ala133=