Linked Data
ClinVar Variation Id:
1036102
ClinVar RCV Id:
RCV001339055
dbSNP Id:
rs2097753511
gnomAD v4:
X-32343261-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.32343261T>A , CM000685.2:g.32343261T>A | GRCh38 |
| NC_000023.10:g.32361378T>A , CM000685.1:g.32361378T>A | GRCh37 |
| NC_000023.9:g.32271299T>A | NCBI36 |
| NG_012232.1:g.1001349A>T , LRG_199:g.1001349A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000358062.7:c.458A>T | ENSP00000350765.3:p.Lys153Met | |
| ENST00000357033.9:c.5612A>T MANE Select | ENSP00000354923.3:p.Lys1871Met | |
| ENST00000619831.5:c.1580A>T | ENSP00000479270.2:p.Lys527Met | |
| ENST00000357033.8:c.5612A>T | ENSP00000354923.3:p.Lys1871Met | |
| ENST00000378677.6:c.5600A>T | ENSP00000367948.2:p.Lys1867Met | |
| ENST00000488902.5:n.336-126198A>T | ||
| ENST00000493412.1:c.269A>T | ENSP00000417725.1:p.Lys90Met | |
| ENST00000619831.4:c.5600A>T | ENSP00000479270.1:p.Lys1867Met | |
| ENST00000620040.4:c.5612A>T | ENSP00000478150.1:p.Lys1871Met | |
| NM_000109.3:c.5588A>T | NP_000100.2:p.Lys1863Met | |
| NM_004006.2:c.5612A>T , LRG_199t1:c.5612A>T | NP_003997.1:p.Lys1871Met | |
| NM_004009.3:c.5600A>T | NP_004000.1:p.Lys1867Met | |
| NM_004010.3:c.5243A>T | NP_004001.1:p.Lys1748Met | |
| NM_004011.3:c.1589A>T | NP_004002.2:p.Lys530Met | |
| NM_004012.3:c.1580A>T | NP_004003.1:p.Lys527Met | |
| XM_006724468.2:c.5612A>T | XP_006724531.1:p.Lys1871Met | |
| XM_006724469.2:c.5588A>T | XP_006724532.1:p.Lys1863Met | |
| XM_006724470.2:c.5612A>T | XP_006724533.1:p.Lys1871Met | |
| XM_006724471.2:c.5612A>T | XP_006724534.1:p.Lys1871Met | |
| XM_006724472.2:c.5483A>T | XP_006724535.1:p.Lys1828Met | |
| XM_006724473.2:c.5474A>T | XP_006724536.1:p.Lys1825Met | |
| XM_006724474.2:c.5612A>T | XP_006724537.1:p.Lys1871Met | |
| XM_006724475.2:c.5612A>T | XP_006724538.1:p.Lys1871Met | |
| XM_011545467.1:c.5489A>T | XP_011543769.1:p.Lys1830Met | |
| XM_011545468.1:c.5612A>T | XP_011543770.1:p.Lys1871Met | |
| XM_011545469.1:c.5612A>T | XP_011543771.1:p.Lys1871Met | |
| XM_006724469.3:c.5588A>T | XP_006724532.1:p.Lys1863Met | |
| XM_006724470.3:c.5612A>T | XP_006724533.1:p.Lys1871Met | |
| XM_006724474.3:c.5612A>T | XP_006724537.1:p.Lys1871Met | |
| XM_011545468.2:c.5612A>T | XP_011543770.1:p.Lys1871Met | |
| XM_017029328.1:c.5612A>T | XP_016884817.1:p.Lys1871Met | |
| XM_017029329.1:c.5612A>T | XP_016884818.1:p.Lys1871Met | |
| XM_017029330.2:c.5612A>T | XP_016884819.1:p.Lys1871Met | |
| NM_000109.4:c.5588A>T | NP_000100.3:p.Lys1863Met | |
| NM_004006.3:c.5612A>T MANE Select | NP_003997.2:p.Lys1871Met | |
| NM_004011.4:c.1589A>T | NP_004002.3:p.Lys530Met | |
| NM_004012.4:c.1580A>T | NP_004003.2:p.Lys527Met |