Linked Data
ClinVar Variation Id:
1329743
dbSNP Id:
rs1364503444
gnomAD v2:
22-38528938-A-G
gnomAD v3:
22-38132931-A-G
gnomAD v4:
22-38132931-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.38132931A>G , CM000684.2:g.38132931A>G | GRCh38 |
| NC_000022.10:g.38528938A>G , CM000684.1:g.38528938A>G | GRCh37 |
| NC_000022.9:g.36858884A>G | NCBI36 |
| NG_007094.2:g.77760T>C | |
| NG_007094.3:g.86848T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000332509.8:c.977T>C MANE Select | ENSP00000333142.3:p.Met326Thr | |
| ENST00000427114.6:c.443T>C | ENSP00000407743.2:p.Met148Thr | |
| ENST00000436218.6:c.*337T>C | ENSP00000401242.1:n.*337T>C | |
| ENST00000655142.1:c.789T>C | ENSP00000499715.1:p.Asp263= | |
| ENST00000660610.1:c.977T>C | ENSP00000499555.1:p.Met326Thr | |
| ENST00000663895.1:c.977T>C | ENSP00000499712.1:p.Met326Thr | |
| ENST00000664587.1:c.977T>C | ENSP00000499394.1:p.Met326Thr | |
| ENST00000665987.1:c.*878T>C | ENSP00000499423.1:n.*878T>C | |
| ENST00000667521.1:c.977T>C | ENSP00000499665.1:p.Met326Thr | |
| ENST00000668208.1:n.1107T>C | ||
| ENST00000668499.1:c.*808T>C | ENSP00000499626.1:n.*808T>C | |
| ENST00000668949.1:c.977T>C | ENSP00000499711.1:p.Met326Thr | |
| ENST00000671093.1:n.1071T>C | ||
| ENST00000673413.1:c.*808T>C | ENSP00000500600.1:n.*808T>C | |
| ENST00000332509.7:c.977T>C | ENSP00000333142.3:p.Met326Thr | |
| ENST00000335539.7:c.977T>C | ENSP00000335149.3:p.Met326Thr | |
| ENST00000402064.5:c.977T>C | ENSP00000386100.1:p.Met326Thr | |
| ENST00000427114.5:c.391T>C | ||
| ENST00000427453.5:c.232T>C | ||
| ENST00000448094.5:c.158T>C | ENSP00000407106.1:p.Met53Thr | |
| ENST00000452542.5:c.469T>C | ||
| ENST00000471636.5:n.413-6404T>C | ||
| NM_001004426.1:c.977T>C | NP_001004426.1:p.Met326Thr | |
| NM_001199562.1:c.977T>C | NP_001186491.1:p.Met326Thr | |
| NM_003560.2:c.977T>C | NP_003551.2:p.Met326Thr | |
| XM_005261764.1:c.977T>C | XP_005261821.1:p.Met326Thr | |
| XM_005261765.1:c.977T>C | XP_005261822.1:p.Met326Thr | |
| XM_005261766.1:c.977T>C | XP_005261823.1:p.Met326Thr | |
| XM_005261771.3:c.977T>C | XP_005261828.1:p.Met326Thr | |
| XM_006724332.2:c.977T>C | XP_006724395.1:p.Met326Thr | |
| XM_011530422.1:c.872T>C | XP_011528724.1:p.Met291Thr | |
| XM_011530423.1:c.443T>C | XP_011528725.1:p.Met148Thr | |
| XM_011530424.1:c.443T>C | XP_011528726.1:p.Met148Thr | |
| XM_011530425.1:c.443T>C | XP_011528727.1:p.Met148Thr | |
| XM_011530426.1:c.977T>C | XP_011528728.1:p.Met326Thr | |
| XM_011530427.1:c.872T>C | XP_011528729.1:p.Met291Thr | |
| XM_011530428.1:c.977T>C | XP_011528730.1:p.Met326Thr | |
| XR_244390.1:n.1085T>C | ||
| XR_244392.1:n.1085T>C | ||
| XR_430411.1:n.1085T>C | ||
| XR_430412.1:n.1085T>C | ||
| XR_937937.1:n.1085T>C | ||
| XR_937938.1:n.1085T>C | ||
| XR_937939.1:n.1085T>C | ||
| XR_937940.1:n.1085T>C | ||
| NM_001004426.2:c.977T>C | NP_001004426.1:p.Met326Thr | |
| NM_001199562.2:c.977T>C | NP_001186491.1:p.Met326Thr | |
| NM_001349864.1:c.977T>C | NP_001336793.1:p.Met326Thr | |
| NM_001349865.1:c.977T>C | NP_001336794.1:p.Met326Thr | |
| NM_001349866.1:c.977T>C | NP_001336795.1:p.Met326Thr | |
| NM_001349867.1:c.443T>C | NP_001336796.1:p.Met148Thr | |
| NM_001349868.1:c.299T>C | NP_001336797.1:p.Met100Thr | |
| NM_001349869.1:c.443T>C | NP_001336798.1:p.Met148Thr | |
| NM_003560.3:c.977T>C | NP_003551.2:p.Met326Thr | |
| XM_005261764.3:c.977T>C | XP_005261821.1:p.Met326Thr | |
| XM_005261765.2:c.977T>C | XP_005261822.1:p.Met326Thr | |
| XM_006724332.4:c.977T>C | XP_006724395.1:p.Met326Thr | |
| XM_011530426.3:c.977T>C | XP_011528728.1:p.Met326Thr | |
| XM_017028983.1:c.443T>C | XP_016884472.1:p.Met148Thr | |
| XM_017028986.2:c.977T>C | XP_016884475.1:p.Met326Thr | |
| XM_017028987.2:c.977T>C | XP_016884476.1:p.Met326Thr | |
| XM_017028988.2:c.977T>C | XP_016884477.1:p.Met326Thr | |
| XM_024452280.1:c.443T>C | XP_024308048.1:p.Met148Thr | |
| XM_024452281.1:c.443T>C | XP_024308049.1:p.Met148Thr | |
| XM_024452282.1:c.443T>C | XP_024308050.1:p.Met148Thr | |
| XM_024452283.1:c.299T>C | XP_024308051.1:p.Met100Thr | |
| XM_024452284.1:c.443T>C | XP_024308052.1:p.Met148Thr | |
| XM_024452285.1:c.443T>C | XP_024308053.1:p.Met148Thr | |
| XR_001755325.2:n.1069T>C | ||
| XR_001755327.2:n.1069T>C | ||
| XR_001755328.2:n.1069T>C | ||
| XR_244390.3:n.1069T>C | ||
| XR_937938.3:n.1069T>C | ||
| XR_937939.3:n.1069T>C | ||
| XR_937940.3:n.1069T>C | ||
| NM_001199562.3:c.977T>C | NP_001186491.1:p.Met326Thr | |
| NM_001349864.2:c.977T>C | NP_001336793.1:p.Met326Thr | |
| NM_001349865.2:c.977T>C | NP_001336794.1:p.Met326Thr | |
| NM_001349866.2:c.977T>C | NP_001336795.1:p.Met326Thr | |
| NM_001349867.2:c.443T>C | NP_001336796.1:p.Met148Thr | |
| NM_001349868.2:c.299T>C | NP_001336797.1:p.Met100Thr | |
| NM_001349869.2:c.443T>C | NP_001336798.1:p.Met148Thr | |
| NM_003560.4:c.977T>C MANE Select | NP_003551.2:p.Met326Thr | |
| NM_001004426.3:c.977T>C | NP_001004426.1:p.Met326Thr |