Linked Data
ClinVar Variation Id:
140985
dbSNP Id:
rs587781417
gnomAD v2:
17-59761459-A-T
gnomAD v4:
17-61684098-A-T
MyVariant Identifiers:
chr17:g.59761459A>T (hg19)
chr17:g.59761459_59761460delinsTT (hg19)
chr17:g.61684098A>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.61684098A>T , CM000679.2:g.61684098A>T | GRCh38 |
| NC_000017.10:g.59761459A>T , CM000679.1:g.59761459A>T | GRCh37 |
| NC_000017.9:g.57116241A>T | NCBI36 |
| NG_007409.2:g.184462T>A , LRG_300:g.184462T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682073.1:n.1688T>A | ||
| ENST00000682453.1:c.2948T>A | ENSP00000506943.1:p.Ile983Asn | |
| ENST00000682477.1:c.*2374T>A | ENSP00000507075.1:n.*2374T>A | |
| ENST00000682589.1:n.8825T>A | ||
| ENST00000682755.1:c.2726T>A | ENSP00000507660.1:p.Ile909Asn | |
| ENST00000682989.1:c.*39T>A | ENSP00000507786.1:n.*39T>A | |
| ENST00000683039.1:c.2948T>A | ENSP00000508303.1:p.Ile983Asn | |
| ENST00000683235.1:c.*363T>A | ENSP00000507646.1:n.*363T>A | |
| ENST00000683535.1:n.1078T>A | ||
| ENST00000684584.1:c.2111T>A | ENSP00000508044.1:p.Ile704Asn | |
| ENST00000684626.1:n.1194T>A | ||
| ENST00000684769.1:c.1138T>A | ENSP00000507691.1:n.1138T>A | |
| ENST00000259008.7:c.2948T>A MANE Select | ENSP00000259008.2:p.Ile983Asn | |
| ENST00000259008.6:c.2948T>A | ENSP00000259008.2:p.Ile983Asn | |
| NM_032043.2:c.2948T>A , LRG_300t1:c.2948T>A | NP_114432.2:p.Ile983Asn | |
| XM_011525332.1:c.3008T>A | XP_011523634.1:p.Ile1003Asn | |
| XM_011525333.1:c.3008T>A | XP_011523635.1:p.Ile1003Asn | |
| XM_011525334.1:c.3008T>A | XP_011523636.1:p.Ile1003Asn | |
| XM_011525335.1:c.2948T>A | XP_011523637.1:p.Ile983Asn | |
| XM_011525336.1:c.2888T>A | XP_011523638.1:p.Ile963Asn | |
| XM_011525337.1:c.2807T>A | XP_011523639.1:p.Ile936Asn | |
| XM_011525338.1:c.2525T>A | XP_011523640.1:p.Ile842Asn | |
| XM_011525332.3:c.3008T>A | XP_011523634.1:p.Ile1003Asn | |
| XM_011525333.3:c.3008T>A | XP_011523635.1:p.Ile1003Asn | |
| XM_011525334.2:c.3008T>A | XP_011523636.1:p.Ile1003Asn | |
| XM_011525335.3:c.2948T>A | XP_011523637.1:p.Ile983Asn | |
| XM_011525336.2:c.2888T>A | XP_011523638.1:p.Ile963Asn | |
| XM_011525337.2:c.2807T>A | XP_011523639.1:p.Ile936Asn | |
| XM_011525338.2:c.2525T>A | XP_011523640.1:p.Ile842Asn | |
| XM_017025200.1:c.2465T>A | XP_016880689.1:p.Ile822Asn | |
| XM_017025201.1:c.2465T>A | XP_016880690.1:p.Ile822Asn | |
| XM_017025202.1:c.1094T>A | XP_016880691.1:p.Ile365Asn | |
| XM_017025203.1:c.1094T>A | XP_016880692.1:p.Ile365Asn | |
| NM_032043.3:c.2948T>A MANE Select | NP_114432.2:p.Ile983Asn |