Canonical Allele Identifier: CA2821714897
Gene: TEX11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.70853351T>A , CM000685.2:g.70853351T>A GRCh38
NC_000023.10:g.70073201T>A , CM000685.1:g.70073201T>A GRCh37
NC_000023.9:g.69989926T>A NCBI36
NG_012574.1:g.60367A>T
NG_012574.2:g.60367A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000374333.7:c.325-23A>T MANE Select ENSP00000363453.2:n.325-23A>T
ENST00000344304.3:c.370-23A>T ENSP00000340995.3:n.370-23A>T
ENST00000374333.6:c.325-23A>T ENSP00000363453.2:n.325-23A>T
ENST00000395889.6:c.370-23A>T ENSP00000379226.2:n.370-23A>T
NM_001003811.1:c.370-23A>T NP_001003811.1:n.370-23A>T
NM_031276.2:c.325-23A>T NP_112566.2:n.325-23A>T
XM_011530994.1:c.325-23A>T XP_011529296.1:n.325-23A>T
XM_017029649.1:c.325-23A>T XP_016885138.1:n.325-23A>T
NM_001003811.2:c.370-23A>T NP_001003811.1:n.370-23A>T
NM_031276.3:c.325-23A>T MANE Select NP_112566.2:n.325-23A>T