Linked Data
ClinVar Variation Id:
762682
ClinVar RCV Id:
RCV001414039
dbSNP Id:
rs1597597640
MyVariant Identifiers:
chr17:g.15134330A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.15231013A>G , CM000679.2:g.15231013A>G | GRCh38 |
| NC_000017.10:g.15134330A>G , CM000679.1:g.15134330A>G | GRCh37 |
| NC_000017.9:g.15075055A>G | NCBI36 |
| NG_007949.1:g.39315T>C , LRG_263:g.39315T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000312280.9:c.387T>C MANE Select | ENSP00000308937.3:p.Asp129= | |
| ENST00000395936.7:c.*96T>C | ENSP00000379268.1:n.*96T>C | |
| ENST00000395938.7:c.376T>C | ENSP00000379269.3:p.Leu126= | |
| ENST00000494511.7:c.183T>C | ENSP00000462782.2:p.Asp61= | |
| ENST00000580584.3:c.183T>C | ENSP00000464468.3:p.Asp61= | |
| ENST00000612492.5:c.387T>C | ENSP00000484631.1:p.Asp129= | |
| ENST00000643451.2:c.*242T>C | ENSP00000494628.1:n.*242T>C | |
| ENST00000644020.1:c.*96T>C | ENSP00000496522.1:n.*96T>C | |
| ENST00000646419.2:c.*96T>C | ENSP00000494871.1:n.*96T>C | |
| ENST00000674651.1:c.387T>C | ENSP00000501727.1:p.Asp129= | |
| ENST00000674673.1:c.387T>C | ENSP00000501804.1:p.Asp129= | |
| ENST00000674707.1:c.183T>C | ENSP00000502250.1:p.Asp61= | |
| ENST00000674868.1:c.387T>C | ENSP00000502835.1:p.Asp129= | |
| ENST00000674871.1:n.403T>C | ||
| ENST00000674947.1:c.376T>C | ENSP00000501580.1:p.Leu126= | |
| ENST00000675197.1:n.367T>C | ||
| ENST00000675350.1:c.387T>C | ENSP00000501557.1:p.Asp129= | |
| ENST00000675551.1:c.*56T>C | ENSP00000501945.1:n.*56T>C | |
| ENST00000675808.1:c.387T>C | ENSP00000502310.1:p.Asp129= | |
| ENST00000675819.1:c.387T>C | ENSP00000502018.1:p.Asp129= | |
| ENST00000675854.1:c.183T>C | ENSP00000502324.1:p.Asp61= | |
| ENST00000675950.1:c.387T>C | ENSP00000501546.1:p.Asp129= | |
| ENST00000676002.1:n.380T>C | ||
| ENST00000676161.1:c.246T>C | ENSP00000501766.1:p.Asp82= | |
| ENST00000676221.1:c.387T>C | ENSP00000502601.1:p.Asp129= | |
| ENST00000676329.1:c.489T>C | ENSP00000501698.1:p.Asp163= | |
| ENST00000312280.7:c.387T>C | ENSP00000308937.3:p.Asp129= | |
| ENST00000395936.5:c.*96T>C | ENSP00000379268.1:n.*96T>C | |
| ENST00000395938.6:c.387T>C | ENSP00000379269.2:p.Asp129= | |
| ENST00000494511.5:c.208T>C | ENSP00000462782.1:p.Leu70= | |
| ENST00000612492.4:c.387T>C | ENSP00000484631.1:p.Asp129= | |
| NM_000304.3:c.387T>C | NP_000295.1:p.Asp129= | |
| NM_001281455.1:c.387T>C | NP_001268384.1:p.Asp129= | |
| NM_001281456.1:c.387T>C | NP_001268385.1:p.Asp129= | |
| NM_153321.2:c.387T>C | NP_696996.1:p.Asp129= | |
| NM_153322.2:c.387T>C | NP_696997.1:p.Asp129= | |
| NR_104017.1:n.513T>C | ||
| NR_104018.1:n.413T>C | ||
| NM_000304.4:c.387T>C MANE Select | NP_000295.1:p.Asp129= | |
| NM_001281456.2:c.387T>C | NP_001268385.1:p.Asp129= | |
| NM_153321.3:c.387T>C | NP_696996.1:p.Asp129= | |
| NM_153322.3:c.387T>C | NP_696997.1:p.Asp129= | |
| NR_104017.2:n.482T>C | ||
| NR_104018.2:n.382T>C | ||
| NM_001281455.2:c.387T>C | NP_001268384.1:p.Asp129= |