Linked Data
ClinVar Variation Id:
318332
dbSNP Id:
rs886051795
gnomAD v2:
16-2136365-G-A
gnomAD v3:
16-2086364-G-A
gnomAD v4:
16-2086364-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.2086364G>A , CM000678.2:g.2086364G>A | GRCh38 |
| NC_000016.9:g.2136365G>A , CM000678.1:g.2136365G>A | GRCh37 |
| NC_000016.8:g.2076366G>A | NCBI36 |
| NG_005895.1:g.42059G>A , LRG_487:g.42059G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000568566.6:c.*3183G>A | ENSP00000455997.2:n.*3183G>A | |
| ENST00000642206.2:c.4681G>A | ENSP00000495146.2:p.Asp1561Asn | |
| ENST00000642365.2:c.4831G>A | ENSP00000495459.2:p.Asp1611Asn | |
| ENST00000644417.2:c.*5347G>A | ENSP00000493912.2:n.*5347G>A | |
| ENST00000646464.2:c.*7583G>A | ENSP00000496610.2:n.*7583G>A | |
| ENST00000219476.9:c.4834G>A MANE Select | ENSP00000219476.3:p.Asp1612Asn | |
| ENST00000350773.9:c.4765G>A | ENSP00000344383.4:p.Asp1589Asn | |
| ENST00000401874.7:c.4633G>A | ENSP00000384468.2:p.Asp1545Asn | |
| ENST00000568454.6:c.4666G>A | ENSP00000454487.1:p.Asp1556Asn | |
| ENST00000569110.2:c.1057G>A | ||
| ENST00000569930.2:n.2716G>A | ||
| ENST00000642365.1:c.3488G>A | ||
| ENST00000642561.1:c.4705G>A | ENSP00000495099.1:p.Asp1569Asn | |
| ENST00000642728.1:n.1016G>A | ||
| ENST00000642791.1:n.431G>A | ||
| ENST00000642797.1:c.4636G>A | ENSP00000493846.1:p.Asp1546Asn | |
| ENST00000642936.1:c.4702G>A | ENSP00000494514.1:p.Asp1568Asn | |
| ENST00000643088.1:c.4627G>A | ENSP00000494747.1:p.Asp1543Asn | |
| ENST00000643177.1:n.848G>A | ||
| ENST00000643426.1:n.2482G>A | ||
| ENST00000643946.1:c.4759G>A | ENSP00000495927.1:p.Asp1587Asn | |
| ENST00000644043.1:c.4705G>A | ENSP00000496262.1:p.Asp1569Asn | |
| ENST00000644278.1:n.316G>A | ||
| ENST00000644329.1:c.4633G>A | ENSP00000496611.1:p.Asp1545Asn | |
| ENST00000644335.1:c.4630G>A | ENSP00000496317.1:p.Asp1544Asn | |
| ENST00000644399.1:c.4755G>A | ||
| ENST00000645024.1:n.2918G>A | ||
| ENST00000646388.1:c.4828G>A | ENSP00000495921.1:p.Asp1610Asn | |
| ENST00000646634.1:n.3649G>A | ||
| ENST00000646674.1:n.2086G>A | ||
| ENST00000647042.1:n.2057G>A | ||
| ENST00000647180.1:n.1947G>A | ||
| ENST00000219476.7:c.4834G>A | ENSP00000219476.3:p.Asp1612Asn | |
| ENST00000350773.8:c.4765G>A | ENSP00000344383.4:p.Asp1589Asn | |
| ENST00000382538.10:c.4489G>A | ENSP00000371978.6:p.Asp1497Asn | |
| ENST00000401874.6:c.4633G>A | ENSP00000384468.2:p.Asp1545Asn | |
| ENST00000439117.6:c.*4001G>A | ENSP00000406980.2:n.*4001G>A | |
| ENST00000439673.6:c.4525G>A | ENSP00000399232.2:p.Asp1509Asn | |
| ENST00000497886.5:n.2592G>A | ||
| ENST00000568454.5:c.4666G>A | ENSP00000454487.1:p.Asp1556Asn | |
| ENST00000569110.1:c.1016G>A | ||
| ENST00000569930.1:n.1949G>A | ||
| NM_000548.3:c.4834G>A , LRG_487t1:c.4834G>A | NP_000539.2:p.Asp1612Asn | |
| NM_001077183.1:c.4633G>A | NP_001070651.1:p.Asp1545Asn | |
| NM_001114382.1:c.4765G>A | NP_001107854.1:p.Asp1589Asn | |
| XM_005255529.3:c.4705G>A | XP_005255586.2:p.Asp1569Asn | |
| XM_005255531.3:c.4636G>A | XP_005255588.2:p.Asp1546Asn | |
| XM_011522636.1:c.4888G>A | XP_011520938.1:p.Asp1630Asn | |
| XM_011522637.1:c.4885G>A | XP_011520939.1:p.Asp1629Asn | |
| XM_011522638.1:c.4777G>A | XP_011520940.1:p.Asp1593Asn | |
| XM_011522639.1:c.4759G>A | XP_011520941.1:p.Asp1587Asn | |
| XM_011522640.1:c.4756G>A | XP_011520942.1:p.Asp1586Asn | |
| XM_011522641.1:c.4525G>A | XP_011520943.1:p.Asp1509Asn | |
| NM_000548.4:c.4834G>A | NP_000539.2:p.Asp1612Asn | |
| NM_001077183.2:c.4633G>A | NP_001070651.1:p.Asp1545Asn | |
| NM_001114382.2:c.4765G>A | NP_001107854.1:p.Asp1589Asn | |
| NM_001318827.1:c.4525G>A | NP_001305756.1:p.Asp1509Asn | |
| NM_001318829.1:c.4489G>A | NP_001305758.1:p.Asp1497Asn | |
| NM_001318831.1:c.4102G>A | NP_001305760.1:p.Asp1368Asn | |
| NM_001318832.1:c.4666G>A | NP_001305761.1:p.Asp1556Asn | |
| NM_001363528.1:c.4636G>A | NP_001350457.1:p.Asp1546Asn | |
| NM_021055.2:c.4705G>A | NP_066399.2:p.Asp1569Asn | |
| XM_005255531.4:c.4636G>A | XP_005255588.2:p.Asp1546Asn | |
| XM_011522636.2:c.4888G>A | XP_011520938.1:p.Asp1630Asn | |
| XM_011522637.2:c.4885G>A | XP_011520939.1:p.Asp1629Asn | |
| XM_011522638.2:c.5050G>A | XP_011520940.2:p.Asp1684Asn | |
| XM_011522639.2:c.4759G>A | XP_011520941.1:p.Asp1587Asn | |
| XM_011522640.2:c.4756G>A | XP_011520942.1:p.Asp1586Asn | |
| XM_017023615.1:c.4831G>A | XP_016879104.1:p.Asp1611Asn | |
| XM_017023616.1:c.4702G>A | XP_016879105.1:p.Asp1568Asn | |
| XM_017023617.1:c.4798G>A | XP_016879106.1:p.Asp1600Asn | |
| XM_017023618.1:c.3544G>A | XP_016879107.1:p.Asp1182Asn | |
| XM_024450413.1:c.4633G>A | XP_024306181.1:p.Asp1545Asn | |
| NM_000548.5:c.4834G>A MANE Select | NP_000539.2:p.Asp1612Asn | |
| NM_001370404.1:c.4702G>A | NP_001357333.1:p.Asp1568Asn | |
| NM_001370405.1:c.4705G>A | NP_001357334.1:p.Asp1569Asn | |
| NM_001077183.3:c.4633G>A | NP_001070651.1:p.Asp1545Asn | |
| NM_001114382.3:c.4765G>A | NP_001107854.1:p.Asp1589Asn | |
| NM_001318827.2:c.4525G>A | NP_001305756.1:p.Asp1509Asn | |
| NM_001318829.2:c.4489G>A | NP_001305758.1:p.Asp1497Asn | |
| NM_001318831.2:c.4102G>A | NP_001305760.1:p.Asp1368Asn | |
| NM_001318832.2:c.4666G>A | NP_001305761.1:p.Asp1556Asn | |
| NM_001363528.2:c.4636G>A | NP_001350457.1:p.Asp1546Asn | |
| NM_021055.3:c.4705G>A | NP_066399.2:p.Asp1569Asn |