Canonical Allele Identifier: CA2436261248
Gene: TEX11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.70853183C= , CM000685.2:g.70853183C= GRCh38
NC_000023.10:g.70073033C= , CM000685.1:g.70073033C= GRCh37
NC_000023.9:g.69989758C= NCBI36
NG_012574.1:g.60535G=
NG_012574.2:g.60535G=

Transcript Alleles

HGVS Amino-acid change
ENST00000374333.7:c.406-30G= MANE Select ENSP00000363453.2:n.406-30G=
ENST00000344304.3:c.451-30G= ENSP00000340995.3:n.451-30G=
ENST00000374333.6:c.406-30G= ENSP00000363453.2:n.406-30G=
ENST00000395889.6:c.451-30G= ENSP00000379226.2:n.451-30G=
NM_001003811.1:c.451-30G= NP_001003811.1:n.451-30G=
NM_031276.2:c.406-30G= NP_112566.2:n.406-30G=
XM_011530994.1:c.406-30G= XP_011529296.1:n.406-30G=
XM_017029649.1:c.406-30G= XP_016885138.1:n.406-30G=
NM_001003811.2:c.451-30G= NP_001003811.1:n.451-30G=
NM_031276.3:c.406-30G= MANE Select NP_112566.2:n.406-30G=