Revel Score:
ENST00000085219 (MANE Select)
0.013
ENST00000536635
0.013
ENST00000341773
0.013
ENST00000419549
0.013
gnomAD v3:
gnomAD v4:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.35345627G>C , CM000681.2:g.35345627G>C | GRCh38 |
| NC_000019.9:g.35836530G>C , CM000681.1:g.35836530G>C | GRCh37 |
| NC_000019.8:g.40528370G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000085219.10:c.2234G>C (CD22) MANE Select | ENSP00000085219.4:p.Gly745Ala | |
| ENST00000085219.9:c.2234G>C (CD22) | ENSP00000085219.4:p.Gly745Ala | |
| ENST00000270311.10:c.1703G>C (CD22) | ENSP00000270311.7:p.Gly568Ala | |
| ENST00000341773.10:c.1703G>C (CD22) | ENSP00000339349.6:p.Gly568Ala | |
| ENST00000419549.6:c.1718G>C (CD22) | ENSP00000403822.2:p.Gly573Ala | |
| ENST00000536635.6:c.1970G>C (CD22) | ENSP00000442279.1:p.Gly657Ala | |
| ENST00000544992.6:c.2208+501G>C (CD22) | ENSP00000441237.1:n.2208+501G>C | |
| ENST00000594250.5:c.1703G>C (CD22) | ENSP00000469984.1:p.Gly568Ala | |
| ENST00000601769.5:c.*1539G>C (CD22) | ENSP00000470193.1:n.*1539G>C | |
| NM_001185099.1:c.1970G>C (CD22) | NP_001172028.1:p.Gly657Ala | |
| NM_001185100.1:c.2208+501G>C (CD22) | NP_001172029.1:n.2208+501G>C | |
| NM_001185101.1:c.1703G>C (CD22) | NP_001172030.1:p.Gly568Ala | |
| NM_001278417.1:c.1718G>C (CD22) | NP_001265346.1:p.Gly573Ala | |
| NM_001771.3:c.2234G>C (CD22) | NP_001762.2:p.Gly745Ala | |
| NR_049828.1:n.115G>C (MIR5196) | ||
| NM_001771.4:c.2234G>C (CD22) MANE Select | NP_001762.2:p.Gly745Ala | |
| NM_001185099.2:c.1970G>C (CD22) | NP_001172028.1:p.Gly657Ala | |
| NM_001185100.2:c.2208+501G>C (CD22) | NP_001172029.1:n.2208+501G>C | |
| NM_001278417.2:c.1718G>C (CD22) | NP_001265346.1:p.Gly573Ala | |
| NM_001185101.2:c.1703G>C (CD22) | NP_001172030.1:p.Gly568Ala |