Linked Data
ClinVar Variation Id:
286909
dbSNP Id:
rs137905486
ExAC:
X:31341774 C / T
gnomAD v2:
X-31341774-C-T
gnomAD v3:
X-31323657-C-T
gnomAD v4:
X-31323657-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.31323657C>T , CM000685.2:g.31323657C>T | GRCh38 |
| NC_000023.10:g.31341774C>T , CM000685.1:g.31341774C>T | GRCh37 |
| NC_000023.9:g.31251695C>T | NCBI36 |
| NG_012232.1:g.2020953G>A , LRG_199:g.2020953G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000358062.7:c.4011G>A | ENSP00000350765.3:p.Thr1337= | |
| ENST00000682238.1:c.1785G>A | ENSP00000508124.1:p.Thr595= | |
| ENST00000683675.1:n.264G>A | ||
| ENST00000683957.1:n.2657G>A | ||
| ENST00000684130.1:c.1785G>A | ENSP00000508037.1:p.Thr595= | |
| ENST00000343523.7:c.1020G>A | ENSP00000340057.4:p.Thr340= | |
| ENST00000357033.9:c.9165G>A MANE Select | ENSP00000354923.3:p.Thr3055= | |
| ENST00000619831.5:c.5133G>A | ENSP00000479270.2:p.Thr1711= | |
| ENST00000620040.5:c.1785G>A | ENSP00000478150.2:p.Thr595= | |
| ENST00000680961.1:c.1785G>A | ENSP00000506386.1:p.Thr595= | |
| ENST00000681646.1:n.2826G>A | ||
| ENST00000343523.6:c.978G>A | ENSP00000340057.3:p.Thr326= | |
| ENST00000357033.8:c.9165G>A | ENSP00000354923.3:p.Thr3055= | |
| ENST00000358062.6:c.2253G>A | ENSP00000350765.2:p.Thr751= | |
| ENST00000359836.5:c.1785G>A | ENSP00000352894.1:p.Thr595= | |
| ENST00000378677.6:c.9153G>A | ENSP00000367948.2:p.Thr3051= | |
| ENST00000378707.7:c.1785G>A | ENSP00000367979.3:p.Thr595= | |
| ENST00000469142.1:n.184G>A | ||
| ENST00000474231.5:c.1785G>A | ENSP00000417123.1:p.Thr595= | |
| ENST00000541735.5:c.1785G>A | ENSP00000444119.1:p.Thr595= | |
| ENST00000619831.4:c.9150G>A | ENSP00000479270.1:p.Thr3050= | |
| ENST00000620040.4:c.9162G>A | ENSP00000478150.1:p.Thr3054= | |
| NM_000109.3:c.9141G>A | NP_000100.2:p.Thr3047= | |
| NM_004006.2:c.9165G>A , LRG_199t1:c.9165G>A | NP_003997.1:p.Thr3055= | |
| NM_004009.3:c.9153G>A | NP_004000.1:p.Thr3051= | |
| NM_004010.3:c.8796G>A | NP_004001.1:p.Thr2932= | |
| NM_004011.3:c.5142G>A | NP_004002.2:p.Thr1714= | |
| NM_004012.3:c.5133G>A | NP_004003.1:p.Thr1711= | |
| NM_004013.2:c.1785G>A | NP_004004.1:p.Thr595= | |
| NM_004014.2:c.978G>A | NP_004005.1:p.Thr326= | |
| NM_004020.3:c.1785G>A | NP_004011.2:p.Thr595= | |
| NM_004021.2:c.1785G>A | NP_004012.1:p.Thr595= | |
| NM_004022.2:c.1785G>A | NP_004013.1:p.Thr595= | |
| NM_004023.2:c.1785G>A | NP_004014.1:p.Thr595= | |
| XM_006724468.2:c.9165G>A | XP_006724531.1:p.Thr3055= | |
| XM_006724469.2:c.9141G>A | XP_006724532.1:p.Thr3047= | |
| XM_006724470.2:c.9165G>A | XP_006724533.1:p.Thr3055= | |
| XM_006724471.2:c.9165G>A | XP_006724534.1:p.Thr3055= | |
| XM_006724472.2:c.9036G>A | XP_006724535.1:p.Thr3012= | |
| XM_006724473.2:c.9027G>A | XP_006724536.1:p.Thr3009= | |
| XM_006724474.2:c.9165G>A | XP_006724537.1:p.Thr3055= | |
| XM_006724475.2:c.9165G>A | XP_006724538.1:p.Thr3055= | |
| XM_011545467.1:c.9042G>A | XP_011543769.1:p.Thr3014= | |
| XM_011545468.1:c.9165G>A | XP_011543770.1:p.Thr3055= | |
| XM_006724469.3:c.9141G>A | XP_006724532.1:p.Thr3047= | |
| XM_006724470.3:c.9165G>A | XP_006724533.1:p.Thr3055= | |
| XM_006724474.3:c.9165G>A | XP_006724537.1:p.Thr3055= | |
| XM_011545468.2:c.9165G>A | XP_011543770.1:p.Thr3055= | |
| XM_017029328.1:c.9165G>A | XP_016884817.1:p.Thr3055= | |
| XM_017029331.1:c.3339G>A | XP_016884820.1:p.Thr1113= | |
| NM_000109.4:c.9141G>A | NP_000100.3:p.Thr3047= | |
| NM_004006.3:c.9165G>A MANE Select | NP_003997.2:p.Thr3055= | |
| NM_004011.4:c.5142G>A | NP_004002.3:p.Thr1714= | |
| NM_004012.4:c.5133G>A | NP_004003.2:p.Thr1711= | |
| NM_004021.3:c.1785G>A | NP_004012.2:p.Thr595= | |
| NM_004023.3:c.1785G>A | NP_004014.2:p.Thr595= | |
| NM_004013.3:c.1785G>A | NP_004004.2:p.Thr595= | |
| NM_004014.3:c.978G>A | NP_004005.2:p.Thr326= | |
| NM_004020.4:c.1785G>A | NP_004011.3:p.Thr595= | |
| NM_004022.3:c.1785G>A | NP_004013.2:p.Thr595= |