Canonical Allele Identifier: CA2203255565

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.4333454G= , CM000678.2:g.4333454G= GRCh38
NC_000016.9:g.4383455G= , CM000678.1:g.4383455G= GRCh37
NC_000016.8:g.4323456G= NCBI36
NG_016391.1:g.6231G=
NG_016391.2:g.23694G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000433375.2:c.280G= (GLIS2) MANE Select ENSP00000395547.1:p.Gly94=
ENST00000262366.7:c.280G= (GLIS2) ENSP00000262366.3:p.Gly94=
ENST00000433375.1:c.280G= (GLIS2) ENSP00000395547.1:p.Gly94=
ENST00000577031.5:c.292-1680C= (PAM16) ENSP00000459113.1:n.292-1680C=
NM_032575.2:c.280G= (GLIS2) NP_115964.2:p.Gly94=
XM_005255641.3:c.280G= (GLIS2) XP_005255698.1:p.Gly94=
XM_005255642.2:c.280G= (GLIS2) XP_005255699.1:p.Gly94=
NM_001318918.1:c.280G= (GLIS2) NP_001305847.1:p.Gly94=
XM_005255641.4:c.280G= (GLIS2) XP_005255698.1:p.Gly94=
NM_032575.3:c.280G= (GLIS2) MANE Select NP_115964.2:p.Gly94=
NM_001318918.2:c.280G= (GLIS2) NP_001305847.1:p.Gly94=