Linked Data
ClinVar Variation Id:
2029057
ClinVar RCV Id:
RCV002894060
MyVariant Identifiers:
chr17:g.59760732T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.61683371T>C , CM000679.2:g.61683371T>C | GRCh38 |
| NC_000017.10:g.59760732T>C , CM000679.1:g.59760732T>C | GRCh37 |
| NC_000017.9:g.57115514T>C | NCBI36 |
| NG_007409.2:g.185189A>G , LRG_300:g.185189A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682073.1:n.2415A>G | ||
| ENST00000682453.1:c.3675A>G | ENSP00000506943.1:p.Lys1225= | |
| ENST00000682477.1:c.*3101A>G | ENSP00000507075.1:n.*3101A>G | |
| ENST00000682589.1:n.9552A>G | ||
| ENST00000682755.1:c.3453A>G | ENSP00000507660.1:p.Lys1151= | |
| ENST00000682989.1:c.*766A>G | ENSP00000507786.1:n.*766A>G | |
| ENST00000683039.1:c.3675A>G | ENSP00000508303.1:p.Lys1225= | |
| ENST00000683235.1:c.*1090A>G | ENSP00000507646.1:n.*1090A>G | |
| ENST00000683535.1:n.1805A>G | ||
| ENST00000684584.1:c.2838A>G | ENSP00000508044.1:p.Lys946= | |
| ENST00000684626.1:n.1921A>G | ||
| ENST00000684769.1:c.1865A>G | ENSP00000507691.1:n.1865A>G | |
| ENST00000259008.7:c.3675A>G MANE Select | ENSP00000259008.2:p.Lys1225= | |
| ENST00000259008.6:c.3675A>G | ENSP00000259008.2:p.Lys1225= | |
| NM_032043.2:c.3675A>G , LRG_300t1:c.3675A>G | NP_114432.2:p.Lys1225= | |
| XM_011525332.1:c.3735A>G | XP_011523634.1:p.Lys1245= | |
| XM_011525333.1:c.3735A>G | XP_011523635.1:p.Lys1245= | |
| XM_011525334.1:c.3735A>G | XP_011523636.1:p.Lys1245= | |
| XM_011525335.1:c.3675A>G | XP_011523637.1:p.Lys1225= | |
| XM_011525336.1:c.3615A>G | XP_011523638.1:p.Lys1205= | |
| XM_011525337.1:c.3534A>G | XP_011523639.1:p.Lys1178= | |
| XM_011525338.1:c.3252A>G | XP_011523640.1:p.Lys1084= | |
| XM_011525332.3:c.3735A>G | XP_011523634.1:p.Lys1245= | |
| XM_011525333.3:c.3735A>G | XP_011523635.1:p.Lys1245= | |
| XM_011525334.2:c.3735A>G | XP_011523636.1:p.Lys1245= | |
| XM_011525335.3:c.3675A>G | XP_011523637.1:p.Lys1225= | |
| XM_011525336.2:c.3615A>G | XP_011523638.1:p.Lys1205= | |
| XM_011525337.2:c.3534A>G | XP_011523639.1:p.Lys1178= | |
| XM_011525338.2:c.3252A>G | XP_011523640.1:p.Lys1084= | |
| XM_017025200.1:c.3192A>G | XP_016880689.1:p.Lys1064= | |
| XM_017025201.1:c.3192A>G | XP_016880690.1:p.Lys1064= | |
| XM_017025202.1:c.1821A>G | XP_016880691.1:p.Lys607= | |
| XM_017025203.1:c.1821A>G | XP_016880692.1:p.Lys607= | |
| NM_032043.3:c.3675A>G MANE Select | NP_114432.2:p.Lys1225= |