Canonical Allele Identifier: CA2436261299
Gene: TEX11 HGNC NCBI

Linked Data

dbSNP Id: rs2091519225
gnomAD v4: X-70853351-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.70853351T>C , CM000685.2:g.70853351T>C GRCh38
NC_000023.10:g.70073201T>C , CM000685.1:g.70073201T>C GRCh37
NC_000023.9:g.69989926T>C NCBI36
NG_012574.1:g.60367A>G
NG_012574.2:g.60367A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000374333.7:c.325-23A>G MANE Select ENSP00000363453.2:n.325-23A>G
ENST00000344304.3:c.370-23A>G ENSP00000340995.3:n.370-23A>G
ENST00000374333.6:c.325-23A>G ENSP00000363453.2:n.325-23A>G
ENST00000395889.6:c.370-23A>G ENSP00000379226.2:n.370-23A>G
NM_001003811.1:c.370-23A>G NP_001003811.1:n.370-23A>G
NM_031276.2:c.325-23A>G NP_112566.2:n.325-23A>G
XM_011530994.1:c.325-23A>G XP_011529296.1:n.325-23A>G
XM_017029649.1:c.325-23A>G XP_016885138.1:n.325-23A>G
NM_001003811.2:c.370-23A>G NP_001003811.1:n.370-23A>G
NM_031276.3:c.325-23A>G MANE Select NP_112566.2:n.325-23A>G