Linked Data
ClinVar Variation Id:
13965
ClinVar RCV Id:
RCV000014998
RCV000033285
RCV000208416
RCV000235118
RCV000678900
RCV001047900
RCV003150930
RCV003338381
dbSNP Id:
rs180177034
ERepo:
CA279968/MONDO:0015280/004
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.140801536C>G , CM000669.2:g.140801536C>G | GRCh38 |
| NC_000007.13:g.140501336C>G , CM000669.1:g.140501336C>G | GRCh37 |
| NC_000007.12:g.140147805C>G | NCBI36 |
| NG_007873.3:g.128229G>C , LRG_299:g.128229G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000646891.2:c.736G>C MANE Select | ENSP00000493543.1:p.Ala246Pro | |
| ENST00000288602.11:c.736G>C | ENSP00000288602.7:p.Ala246Pro | |
| ENST00000496384.7:c.736G>C | ENSP00000419060.2:p.Ala246Pro | |
| ENST00000497784.2:c.*186G>C | ENSP00000420119.2:n.*186G>C | |
| ENST00000642228.1:c.736G>C | ENSP00000493678.1:p.Ala246Pro | |
| ENST00000642272.1:n.768G>C | ||
| ENST00000642875.1:n.230G>C | ||
| ENST00000643356.1:n.337G>C | ||
| ENST00000644120.1:n.1178G>C | ||
| ENST00000644905.1:n.825G>C | ||
| ENST00000644969.2:c.736G>C MANE Plus Clinical | ENSP00000496776.1:p.Ala246Pro | |
| ENST00000646730.1:c.736G>C | ENSP00000494784.1:p.Ala246Pro | |
| ENST00000646891.1:c.736G>C | ENSP00000493543.1:p.Ala246Pro | |
| ENST00000288602.10:c.736G>C | ENSP00000288602.6:p.Ala246Pro | |
| ENST00000497784.1:c.771G>C | ENSP00000420119.1:n.771G>C | |
| NM_004333.4:c.736G>C , LRG_299t1:c.736G>C | NP_004324.2:p.Ala246Pro | |
| XM_005250045.1:c.736G>C | XP_005250102.1:p.Ala246Pro | |
| XM_005250046.1:c.736G>C | XP_005250103.1:p.Ala246Pro | |
| XM_011516529.1:c.736G>C | XP_011514831.1:p.Ala246Pro | |
| XM_011516530.1:c.736G>C | XP_011514832.1:p.Ala246Pro | |
| XR_242190.1:n.744G>C | ||
| XR_927520.1:n.744G>C | ||
| XR_927521.1:n.744G>C | ||
| XR_927522.1:n.744G>C | ||
| XR_927523.1:n.744G>C | ||
| NM_001354609.1:c.736G>C | NP_001341538.1:p.Ala246Pro | |
| NM_004333.5:c.736G>C | NP_004324.2:p.Ala246Pro | |
| NR_148928.1:n.1041G>C | ||
| XM_017012558.1:c.736G>C | XP_016868047.1:p.Ala246Pro | |
| XM_017012559.1:c.736G>C | XP_016868048.1:p.Ala246Pro | |
| XR_001744857.1:n.744G>C | ||
| XR_001744858.1:n.744G>C | ||
| NM_001354609.2:c.736G>C | NP_001341538.1:p.Ala246Pro | |
| NM_001374244.1:c.736G>C | NP_001361173.1:p.Ala246Pro | |
| NM_001374258.1:c.736G>C MANE Plus Clinical | NP_001361187.1:p.Ala246Pro | |
| NM_004333.6:c.736G>C MANE Select | NP_004324.2:p.Ala246Pro | |
| NM_001378467.1:c.745G>C | NP_001365396.1:p.Ala249Pro | |
| NM_001378468.1:c.736G>C | NP_001365397.1:p.Ala246Pro | |
| NM_001378469.1:c.736G>C | NP_001365398.1:p.Ala246Pro | |
| NM_001378470.1:c.634G>C | NP_001365399.1:p.Ala212Pro | |
| NM_001378471.1:c.736G>C | NP_001365400.1:p.Ala246Pro | |
| NM_001378472.1:c.580G>C | NP_001365401.1:p.Ala194Pro | |
| NM_001378473.1:c.580G>C | NP_001365402.1:p.Ala194Pro | |
| NM_001378474.1:c.736G>C | NP_001365403.1:p.Ala246Pro | |
| NM_001378475.1:c.472G>C | NP_001365404.1:p.Ala158Pro |