Canonical Allele Identifier: CA2436261259
Gene: TEX11 HGNC NCBI

Linked Data

dbSNP Id: rs2091518221
gnomAD v4: X-70853213-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.70853213A>C , CM000685.2:g.70853213A>C GRCh38
NC_000023.10:g.70073063A>C , CM000685.1:g.70073063A>C GRCh37
NC_000023.9:g.69989788A>C NCBI36
NG_012574.1:g.60505T>G
NG_012574.2:g.60505T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000374333.7:c.405+35T>G MANE Select ENSP00000363453.2:n.405+35T>G
ENST00000344304.3:c.450+35T>G ENSP00000340995.3:n.450+35T>G
ENST00000374333.6:c.405+35T>G ENSP00000363453.2:n.405+35T>G
ENST00000395889.6:c.450+35T>G ENSP00000379226.2:n.450+35T>G
NM_001003811.1:c.450+35T>G NP_001003811.1:n.450+35T>G
NM_031276.2:c.405+35T>G NP_112566.2:n.405+35T>G
XM_011530994.1:c.405+35T>G XP_011529296.1:n.405+35T>G
XM_017029649.1:c.405+35T>G XP_016885138.1:n.405+35T>G
NM_001003811.2:c.450+35T>G NP_001003811.1:n.450+35T>G
NM_031276.3:c.405+35T>G MANE Select NP_112566.2:n.405+35T>G