Linked Data
dbSNP Id:
rs991842278
gnomAD v3:
10-70600936-G-T
gnomAD v4:
10-70600936-G-T
MyVariant Identifiers:
chr10:g.70600936G>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.70600936G>T , CM000672.2:g.70600936G>T | GRCh38 |
| NC_000010.10:g.72360692G>T , CM000672.1:g.72360692G>T | GRCh37 |
| NC_000010.9:g.72030698G>T | NCBI36 |
| NG_009615.1:g.6840C>A , LRG_94:g.6840C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000697571.1:c.*17+1852G>T (PALD1) | ENSP00000513342.1:n.*17+1852G>T | |
| ENST00000697572.1:c.2250+36417G>T (PALD1) | ENSP00000513343.1:n.2250+36417G>T | |
| ENST00000697573.1:c.*17+1852G>T (PALD1) | ENSP00000513344.1:n.*17+1852G>T | |
| ENST00000697577.1:n.2919+1852G>T (PALD1) | ||
| ENST00000697578.1:n.2763+1852G>T (PALD1) | ||
| ENST00000441259.2:c.-30-4C>A (PRF1) MANE Select | ENSP00000398568.1:n.-30-4C>A | |
| ENST00000638674.1:c.-4-30C>A (PRF1) | ENSP00000492048.1:n.-4-30C>A | |
| ENST00000639390.1:n.97+1709C>A (PRF1) | ||
| ENST00000373209.2:c.-4-30C>A (PRF1) | ENSP00000362305.1:n.-4-30C>A | |
| ENST00000441259.1:c.-30-4C>A (PRF1) | ENSP00000398568.1:n.-30-4C>A | |
| NM_001083116.1:c.-30-4C>A , LRG_94t1:c.-30-4C>A (PRF1) | NP_001076585.1:n.-30-4C>A | |
| NM_005041.4:c.-4-30C>A (PRF1) | NP_005032.2:n.-4-30C>A | |
| NM_001083116.2:c.-30-4C>A (PRF1) | NP_001076585.1:n.-30-4C>A | |
| NM_005041.5:c.-4-30C>A (PRF1) | NP_005032.2:n.-4-30C>A | |
| NM_001083116.3:c.-30-4C>A (PRF1) MANE Select | NP_001076585.1:n.-30-4C>A | |
| NM_005041.6:c.-4-30C>A (PRF1) | NP_005032.2:n.-4-30C>A |