Canonical Allele Identifier: CA413608034
Gene: TEX11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.70853258G>A , CM000685.2:g.70853258G>A GRCh38
NC_000023.10:g.70073108G>A , CM000685.1:g.70073108G>A GRCh37
NC_000023.9:g.69989833G>A NCBI36
NG_012574.1:g.60460C>T
NG_012574.2:g.60460C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000374333.7:c.395C>T MANE Select ENSP00000363453.2:p.Ala132Val
ENST00000344304.3:c.440C>T ENSP00000340995.3:p.Ala147Val
ENST00000374333.6:c.395C>T ENSP00000363453.2:p.Ala132Val
ENST00000395889.6:c.440C>T ENSP00000379226.2:p.Ala147Val
NM_001003811.1:c.440C>T NP_001003811.1:p.Ala147Val
NM_031276.2:c.395C>T NP_112566.2:p.Ala132Val
XM_011530994.1:c.395C>T XP_011529296.1:p.Ala132Val
XM_017029649.1:c.395C>T XP_016885138.1:p.Ala132Val
NM_001003811.2:c.440C>T NP_001003811.1:p.Ala147Val
NM_031276.3:c.395C>T MANE Select NP_112566.2:p.Ala132Val