Canonical Allele Identifier: CA2203255522

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.4333429A= , CM000678.2:g.4333429A= GRCh38
NC_000016.9:g.4383430A= , CM000678.1:g.4383430A= GRCh37
NC_000016.8:g.4323431A= NCBI36
NG_016391.1:g.6206A=
NG_016391.2:g.23669A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000433375.2:c.255A= (GLIS2) MANE Select ENSP00000395547.1:p.Pro85=
ENST00000262366.7:c.255A= (GLIS2) ENSP00000262366.3:p.Pro85=
ENST00000433375.1:c.255A= (GLIS2) ENSP00000395547.1:p.Pro85=
ENST00000577031.5:c.292-1655T= (PAM16) ENSP00000459113.1:n.292-1655T=
NM_032575.2:c.255A= (GLIS2) NP_115964.2:p.Pro85=
XM_005255641.3:c.255A= (GLIS2) XP_005255698.1:p.Pro85=
XM_005255642.2:c.255A= (GLIS2) XP_005255699.1:p.Pro85=
NM_001318918.1:c.255A= (GLIS2) NP_001305847.1:p.Pro85=
XM_005255641.4:c.255A= (GLIS2) XP_005255698.1:p.Pro85=
NM_032575.3:c.255A= (GLIS2) MANE Select NP_115964.2:p.Pro85=
NM_001318918.2:c.255A= (GLIS2) NP_001305847.1:p.Pro85=