Linked Data
ClinVar Variation Id:
366958
dbSNP Id:
rs374929970
ExAC:
9:3898759 G / A
gnomAD v2:
9-3898759-G-A
gnomAD v3:
9-3898759-G-A
gnomAD v4:
9-3898759-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.3898759G>A , CM000671.2:g.3898759G>A | GRCh38 |
| NC_000009.11:g.3898759G>A , CM000671.1:g.3898759G>A | GRCh37 |
| NC_000009.10:g.3888759G>A | NCBI36 |
| NG_011782.1:g.406277C>T | |
| NG_011782.2:g.406277C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000463680.6:n.350C>T (GLIS3) | ||
| ENST00000464391.2:n.618C>T (GLIS3) | ||
| ENST00000491889.6:c.*1423C>T (GLIS3) | ENSP00000419914.1:n.*1423C>T | |
| ENST00000645252.2:n.502C>T (GLIS3) | ||
| ENST00000682749.1:c.1595C>T (GLIS3) | ENSP00000507306.1:p.Ser532Phe | |
| ENST00000682846.1:c.132-69267C>T (GLIS3) | ENSP00000507527.1:n.132-69267C>T | |
| ENST00000682864.1:n.559C>T (GLIS3) | ||
| ENST00000381971.8:c.2060C>T (GLIS3) MANE Select | ENSP00000371398.3:p.Ser687Phe | |
| ENST00000645252.1:n.502C>T (GLIS3) | ||
| ENST00000324333.14:c.1595C>T (GLIS3) | ENSP00000325494.10:p.Ser532Phe | |
| ENST00000381971.7:c.2060C>T (GLIS3) | ENSP00000371398.3:p.Ser687Phe | |
| ENST00000461870.5:n.416C>T (GLIS3) | ||
| ENST00000463680.5:n.350C>T (GLIS3) | ||
| ENST00000467497.6:n.600C>T (GLIS3) | ||
| NM_001042413.1:c.2060C>T (GLIS3) | NP_001035878.1:p.Ser687Phe | |
| NM_152629.3:c.1595C>T (GLIS3) | NP_689842.3:p.Ser532Phe | |
| NR_026663.1:n.114G>A (GLIS3-AS1) | ||
| XM_005251386.3:c.1595C>T (GLIS3) | XP_005251443.1:p.Ser532Phe | |
| XM_005251387.3:c.1394C>T (GLIS3) | XP_005251444.1:p.Ser465Phe | |
| XM_005251388.3:c.1394C>T (GLIS3) | XP_005251445.1:p.Ser465Phe | |
| XM_011517763.1:c.2060C>T (GLIS3) | XP_011516065.1:p.Ser687Phe | |
| XM_011517764.1:c.2060C>T (GLIS3) | XP_011516066.1:p.Ser687Phe | |
| XM_011517765.1:c.2060C>T (GLIS3) | XP_011516067.1:p.Ser687Phe | |
| XM_011517766.1:c.1595C>T (GLIS3) | XP_011516068.1:p.Ser532Phe | |
| XM_011517767.1:c.1394C>T (GLIS3) | XP_011516069.1:p.Ser465Phe | |
| XM_005251386.4:c.1595C>T (GLIS3) | XP_005251443.1:p.Ser532Phe | |
| XM_005251387.4:c.1394C>T (GLIS3) | XP_005251444.1:p.Ser465Phe | |
| XM_005251388.4:c.1394C>T (GLIS3) | XP_005251445.1:p.Ser465Phe | |
| XM_011517763.2:c.2060C>T (GLIS3) | XP_011516065.1:p.Ser687Phe | |
| XM_011517764.2:c.2060C>T (GLIS3) | XP_011516066.1:p.Ser687Phe | |
| XM_011517765.2:c.2060C>T (GLIS3) | XP_011516067.1:p.Ser687Phe | |
| XM_011517766.2:c.1595C>T (GLIS3) | XP_011516068.1:p.Ser532Phe | |
| XM_011517767.3:c.1394C>T (GLIS3) | XP_011516069.1:p.Ser465Phe | |
| XM_017014361.1:c.1595C>T (GLIS3) | XP_016869850.1:p.Ser532Phe | |
| NM_001042413.2:c.2060C>T (GLIS3) MANE Select | NP_001035878.1:p.Ser687Phe | |
| NM_152629.4:c.1595C>T (GLIS3) | NP_689842.3:p.Ser532Phe |