Revel Score:
ENST00000534884
0.085
ENST00000378677
0.085
ENST00000357033 (MANE Select)
0.085
ENST00000542849
0.085
ENST00000535280
0.085
gnomAD v2:
gnomAD v4:
Joint Max Group AF
0.00000716 (NFE)
Exomes Max Group AF
0.00000761 (NFE)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.32448554G>A , CM000685.2:g.32448554G>A | GRCh38 |
| NC_000023.10:g.32466671G>A , CM000685.1:g.32466671G>A | GRCh37 |
| NC_000023.9:g.32376592G>A | NCBI36 |
| NG_012232.1:g.896056C>T , LRG_199:g.896056C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682899.1:n.3895C>T | ||
| ENST00000357033.9:c.3688C>T MANE Select | ENSP00000354923.3:p.Pro1230Ser | |
| ENST00000357033.8:c.3688C>T | ENSP00000354923.3:p.Pro1230Ser | |
| ENST00000378677.6:c.3676C>T | ENSP00000367948.2:p.Pro1226Ser | |
| ENST00000420596.5:c.94-83355C>T | ENSP00000399897.1:n.94-83355C>T | |
| ENST00000448370.5:c.94-83844C>T | ENSP00000388559.1:n.94-83844C>T | |
| ENST00000488902.5:n.336-231491C>T | ||
| ENST00000619831.4:c.3676C>T | ENSP00000479270.1:p.Pro1226Ser | |
| ENST00000620040.4:c.3688C>T | ENSP00000478150.1:p.Pro1230Ser | |
| NM_000109.3:c.3664C>T | NP_000100.2:p.Pro1222Ser | |
| NM_004006.2:c.3688C>T , LRG_199t1:c.3688C>T | NP_003997.1:p.Pro1230Ser | |
| NM_004009.3:c.3676C>T | NP_004000.1:p.Pro1226Ser | |
| NM_004010.3:c.3319C>T | NP_004001.1:p.Pro1107Ser | |
| XM_006724468.2:c.3688C>T | XP_006724531.1:p.Pro1230Ser | |
| XM_006724469.2:c.3664C>T | XP_006724532.1:p.Pro1222Ser | |
| XM_006724470.2:c.3688C>T | XP_006724533.1:p.Pro1230Ser | |
| XM_006724471.2:c.3688C>T | XP_006724534.1:p.Pro1230Ser | |
| XM_006724472.2:c.3559C>T | XP_006724535.1:p.Pro1187Ser | |
| XM_006724473.2:c.3688C>T | XP_006724536.1:p.Pro1230Ser | |
| XM_006724474.2:c.3688C>T | XP_006724537.1:p.Pro1230Ser | |
| XM_006724475.2:c.3688C>T | XP_006724538.1:p.Pro1230Ser | |
| XM_011545467.1:c.3688C>T | XP_011543769.1:p.Pro1230Ser | |
| XM_011545468.1:c.3688C>T | XP_011543770.1:p.Pro1230Ser | |
| XM_011545469.1:c.3688C>T | XP_011543771.1:p.Pro1230Ser | |
| XM_006724469.3:c.3664C>T | XP_006724532.1:p.Pro1222Ser | |
| XM_006724470.3:c.3688C>T | XP_006724533.1:p.Pro1230Ser | |
| XM_006724474.3:c.3688C>T | XP_006724537.1:p.Pro1230Ser | |
| XM_011545468.2:c.3688C>T | XP_011543770.1:p.Pro1230Ser | |
| XM_017029328.1:c.3688C>T | XP_016884817.1:p.Pro1230Ser | |
| XM_017029329.1:c.3688C>T | XP_016884818.1:p.Pro1230Ser | |
| XM_017029330.2:c.3688C>T | XP_016884819.1:p.Pro1230Ser | |
| NM_000109.4:c.3664C>T | NP_000100.3:p.Pro1222Ser | |
| NM_004006.3:c.3688C>T MANE Select | NP_003997.2:p.Pro1230Ser |