Canonical Allele Identifier: CA2436261250
Gene: TEX11 HGNC NCBI

Linked Data

dbSNP Id: rs888423588

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.70853184A>T , CM000685.2:g.70853184A>T GRCh38
NC_000023.10:g.70073034A>T , CM000685.1:g.70073034A>T GRCh37
NC_000023.9:g.69989759A>T NCBI36
NG_012574.1:g.60534T>A
NG_012574.2:g.60534T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000374333.7:c.406-31T>A MANE Select ENSP00000363453.2:n.406-31T>A
ENST00000344304.3:c.451-31T>A ENSP00000340995.3:n.451-31T>A
ENST00000374333.6:c.406-31T>A ENSP00000363453.2:n.406-31T>A
ENST00000395889.6:c.451-31T>A ENSP00000379226.2:n.451-31T>A
NM_001003811.1:c.451-31T>A NP_001003811.1:n.451-31T>A
NM_031276.2:c.406-31T>A NP_112566.2:n.406-31T>A
XM_011530994.1:c.406-31T>A XP_011529296.1:n.406-31T>A
XM_017029649.1:c.406-31T>A XP_016885138.1:n.406-31T>A
NM_001003811.2:c.451-31T>A NP_001003811.1:n.451-31T>A
NM_031276.3:c.406-31T>A MANE Select NP_112566.2:n.406-31T>A