Linked Data
ClinVar Variation Id:
409879
dbSNP Id:
rs377412251
ExAC:
X:32383300 A / G
gnomAD v2:
X-32383300-A-G
gnomAD v3:
X-32365183-A-G
gnomAD v4:
X-32365183-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.32365183A>G , CM000685.2:g.32365183A>G | GRCh38 |
| NC_000023.10:g.32383300A>G , CM000685.1:g.32383300A>G | GRCh37 |
| NC_000023.9:g.32293221A>G | NCBI36 |
| NG_012232.1:g.979427T>C , LRG_199:g.979427T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000357033.9:c.4862T>C MANE Select | ENSP00000354923.3:p.Ile1621Thr | |
| ENST00000619831.5:c.830T>C | ENSP00000479270.2:p.Ile277Thr | |
| ENST00000357033.8:c.4862T>C | ENSP00000354923.3:p.Ile1621Thr | |
| ENST00000378677.6:c.4850T>C | ENSP00000367948.2:p.Ile1617Thr | |
| ENST00000420596.5:c.110T>C | ENSP00000399897.1:p.Ile37Thr | |
| ENST00000448370.5:c.94-473T>C | ENSP00000388559.1:n.94-473T>C | |
| ENST00000488902.5:n.336-148120T>C | ||
| ENST00000619831.4:c.4850T>C | ENSP00000479270.1:p.Ile1617Thr | |
| ENST00000620040.4:c.4862T>C | ENSP00000478150.1:p.Ile1621Thr | |
| NM_000109.3:c.4838T>C | NP_000100.2:p.Ile1613Thr | |
| NM_004006.2:c.4862T>C , LRG_199t1:c.4862T>C | NP_003997.1:p.Ile1621Thr | |
| NM_004009.3:c.4850T>C | NP_004000.1:p.Ile1617Thr | |
| NM_004010.3:c.4493T>C | NP_004001.1:p.Ile1498Thr | |
| NM_004011.3:c.839T>C | NP_004002.2:p.Ile280Thr | |
| NM_004012.3:c.830T>C | NP_004003.1:p.Ile277Thr | |
| XM_006724468.2:c.4862T>C | XP_006724531.1:p.Ile1621Thr | |
| XM_006724469.2:c.4838T>C | XP_006724532.1:p.Ile1613Thr | |
| XM_006724470.2:c.4862T>C | XP_006724533.1:p.Ile1621Thr | |
| XM_006724471.2:c.4862T>C | XP_006724534.1:p.Ile1621Thr | |
| XM_006724472.2:c.4733T>C | XP_006724535.1:p.Ile1578Thr | |
| XM_006724473.2:c.4862T>C | XP_006724536.1:p.Ile1621Thr | |
| XM_006724474.2:c.4862T>C | XP_006724537.1:p.Ile1621Thr | |
| XM_006724475.2:c.4862T>C | XP_006724538.1:p.Ile1621Thr | |
| XM_011545467.1:c.4862T>C | XP_011543769.1:p.Ile1621Thr | |
| XM_011545468.1:c.4862T>C | XP_011543770.1:p.Ile1621Thr | |
| XM_011545469.1:c.4862T>C | XP_011543771.1:p.Ile1621Thr | |
| XM_006724469.3:c.4838T>C | XP_006724532.1:p.Ile1613Thr | |
| XM_006724470.3:c.4862T>C | XP_006724533.1:p.Ile1621Thr | |
| XM_006724474.3:c.4862T>C | XP_006724537.1:p.Ile1621Thr | |
| XM_011545468.2:c.4862T>C | XP_011543770.1:p.Ile1621Thr | |
| XM_017029328.1:c.4862T>C | XP_016884817.1:p.Ile1621Thr | |
| XM_017029329.1:c.4862T>C | XP_016884818.1:p.Ile1621Thr | |
| XM_017029330.2:c.4862T>C | XP_016884819.1:p.Ile1621Thr | |
| NM_000109.4:c.4838T>C | NP_000100.3:p.Ile1613Thr | |
| NM_004006.3:c.4862T>C MANE Select | NP_003997.2:p.Ile1621Thr | |
| NM_004011.4:c.839T>C | NP_004002.3:p.Ile280Thr | |
| NM_004012.4:c.830T>C | NP_004003.2:p.Ile277Thr |