Canonical Allele Identifier: CA413608027
Gene: TEX11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.70853253C>T , CM000685.2:g.70853253C>T GRCh38
NC_000023.10:g.70073103C>T , CM000685.1:g.70073103C>T GRCh37
NC_000023.9:g.69989828C>T NCBI36
NG_012574.1:g.60465G>A
NG_012574.2:g.60465G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000374333.7:c.400G>A MANE Select ENSP00000363453.2:p.Val134Met
ENST00000344304.3:c.445G>A ENSP00000340995.3:p.Val149Met
ENST00000374333.6:c.400G>A ENSP00000363453.2:p.Val134Met
ENST00000395889.6:c.445G>A ENSP00000379226.2:p.Val149Met
NM_001003811.1:c.445G>A NP_001003811.1:p.Val149Met
NM_031276.2:c.400G>A NP_112566.2:p.Val134Met
XM_011530994.1:c.400G>A XP_011529296.1:p.Val134Met
XM_017029649.1:c.400G>A XP_016885138.1:p.Val134Met
NM_001003811.2:c.445G>A NP_001003811.1:p.Val149Met
NM_031276.3:c.400G>A MANE Select NP_112566.2:p.Val134Met