Linked Data
ClinVar Variation Id:
525243
ClinVar RCV Id:
RCV000629292
dbSNP Id:
rs138222058
ExAC:
5:13830835 G / C
gnomAD v2:
5-13830835-G-C
gnomAD v3:
5-13830726-G-C
gnomAD v4:
5-13830726-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.13830726G>C , CM000667.2:g.13830726G>C | GRCh38 |
| NC_000005.9:g.13830835G>C , CM000667.1:g.13830835G>C | GRCh37 |
| NC_000005.8:g.13883835G>C | NCBI36 |
| NG_013081.1:g.118755C>G | |
| NG_013081.2:g.118755C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000683090.1:n.863C>G | ||
| ENST00000265104.5:c.5932C>G MANE Select | ENSP00000265104.4:p.Pro1978Ala | |
| ENST00000681290.1:c.5887C>G | ENSP00000505288.1:p.Pro1963Ala | |
| ENST00000265104.4:c.5932C>G | ENSP00000265104.4:p.Pro1978Ala | |
| NM_001369.2:c.5932C>G | NP_001360.1:p.Pro1978Ala | |
| XM_005248262.2:c.5887C>G | XP_005248319.1:p.Pro1963Ala | |
| XM_011513990.1:c.5932C>G | XP_011512292.1:p.Pro1978Ala | |
| XR_925598.1:n.6139C>G | ||
| XM_005248262.3:c.6040C>G | XP_005248319.2:p.Pro2014Ala | |
| XM_017009177.1:c.6040C>G | XP_016864666.1:p.Pro2014Ala | |
| XM_017009178.1:c.4945C>G | XP_016864667.1:p.Pro1649Ala | |
| XM_017009179.2:c.4945C>G | XP_016864668.1:p.Pro1649Ala | |
| XM_017009180.1:c.6040C>G | XP_016864669.1:p.Pro2014Ala | |
| XM_017009181.1:c.6040C>G | XP_016864670.1:p.Pro2014Ala | |
| XM_017009182.1:c.6040C>G | XP_016864671.1:p.Pro2014Ala | |
| XM_017009183.1:c.6040C>G | XP_016864672.1:p.Pro2014Ala | |
| XM_017009184.1:c.6040C>G | XP_016864673.1:p.Pro2014Ala | |
| XM_017009185.1:c.1129C>G | XP_016864674.1:p.Pro377Ala | |
| XM_017009186.1:c.682C>G | XP_016864675.1:p.Pro228Ala | |
| XM_017009187.1:c.6040C>G | XP_016864676.1:p.Pro2014Ala | |
| XM_017009188.1:c.19C>G | XP_016864677.1:p.Pro7Ala | |
| XM_024454388.1:c.4945C>G | XP_024310156.1:p.Pro1649Ala | |
| XM_024454389.1:c.4534C>G | XP_024310157.1:p.Pro1512Ala | |
| XR_001742034.1:n.6057C>G | ||
| XR_001742035.1:n.6057C>G | ||
| NM_001369.3:c.5932C>G MANE Select | NP_001360.1:p.Pro1978Ala |