Canonical Allele Identifier: CA355011
Gene: TEX11 HGNC NCBI

Linked Data

ClinVar Variation Id: 192381
dbSNP Id: rs147088100
gnomAD v2: X-70073098-G-A
gnomAD v3: X-70853248-G-A
gnomAD v4: X-70853248-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.70853248G>A , CM000685.2:g.70853248G>A GRCh38
NC_000023.10:g.70073098G>A , CM000685.1:g.70073098G>A GRCh37
NC_000023.9:g.69989823G>A NCBI36
NG_012574.1:g.60470C>T
NG_012574.2:g.60470C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000374333.7:c.405C>T MANE Select ENSP00000363453.2:p.Ala135=
ENST00000344304.3:c.450C>T ENSP00000340995.3:p.Ala150=
ENST00000374333.6:c.405C>T ENSP00000363453.2:p.Ala135=
ENST00000395889.6:c.450C>T ENSP00000379226.2:p.Ala150=
NM_001003811.1:c.450C>T NP_001003811.1:p.Ala150=
NM_031276.2:c.405C>T NP_112566.2:p.Ala135=
XM_011530994.1:c.405C>T XP_011529296.1:p.Ala135=
XM_017029649.1:c.405C>T XP_016885138.1:p.Ala135=
NM_001003811.2:c.450C>T NP_001003811.1:p.Ala150=
NM_031276.3:c.405C>T MANE Select NP_112566.2:p.Ala135=