Canonical Allele Identifier: CA2436261249
Gene: TEX11 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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