Linked Data
ClinVar Variation Id:
2693180
ClinVar RCV Id:
RCV003495367
gnomAD v4:
16-88856773-G-T
MyVariant Identifiers:
chr16:g.88923181G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.88856773G>T , CM000678.2:g.88856773G>T | GRCh38 |
| NC_000016.9:g.88923181G>T , CM000678.1:g.88923181G>T | GRCh37 |
| NC_000016.8:g.87450682G>T | NCBI36 |
| NG_008667.1:g.5194C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000268695.10:c.105C>A (GALNS) MANE Select | ENSP00000268695.5:p.Leu35= | |
| ENST00000268695.9:c.105C>A (GALNS) | ENSP00000268695.5:p.Leu35= | |
| ENST00000564365.5:c.-398+527G>T (TRAPPC2L) | ENSP00000455447.1:n.-398+527G>T | |
| ENST00000565364.1:n.70C>A (GALNS) | ||
| ENST00000567525.5:c.54C>A (GALNS) | ENSP00000454484.1:p.Leu18= | |
| ENST00000568311.1:c.105C>A (GALNS) | ENSP00000455006.1:p.Leu35= | |
| ENST00000568613.5:c.54C>A (GALNS) | ENSP00000457921.1:p.Leu18= | |
| ENST00000569433.1:c.105C>A (GALNS) | ENSP00000456884.1:p.Leu35= | |
| NM_000512.4:c.105C>A (GALNS) | NP_000503.1:p.Leu35= | |
| XM_005256301.2:c.105C>A (GALNS) | XP_005256358.1:p.Leu35= | |
| XM_005256302.1:c.-48C>A (GALNS) | XP_005256359.1:n.-48C>A | |
| XM_011522982.1:c.-48C>A (GALNS) | XP_011521284.1:n.-48C>A | |
| XM_011522984.1:c.-48C>A (GALNS) | XP_011521286.1:n.-48C>A | |
| NM_001323543.1:c.-327C>A (GALNS) | NP_001310472.1:n.-327C>A | |
| NM_001323544.1:c.-48C>A (GALNS) | NP_001310473.1:n.-48C>A | |
| NR_134671.1:n.27+527G>T (TRAPPC2L) | ||
| XM_005256301.3:c.105C>A (GALNS) | XP_005256358.1:p.Leu35= | |
| XM_011522982.2:c.-48C>A (GALNS) | XP_011521284.1:n.-48C>A | |
| XM_017023113.1:c.-327C>A (GALNS) | XP_016878602.1:n.-327C>A | |
| NM_000512.5:c.105C>A (GALNS) MANE Select | NP_000503.1:p.Leu35= | |
| NM_001323543.2:c.-327C>A (GALNS) | NP_001310472.1:n.-327C>A | |
| NM_001323544.2:c.-48C>A (GALNS) | NP_001310473.1:n.-48C>A | |
| NR_134671.2:n.27+527G>T (TRAPPC2L) |