Canonical Allele Identifier: CA405331976
Gene: CD22 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35332922C>G , CM000681.2:g.35332922C>G GRCh38
NC_000019.9:g.35823825C>G , CM000681.1:g.35823825C>G GRCh37
NC_000019.8:g.40515665C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000085219.10:c.410C>G MANE Select ENSP00000085219.4:p.Ser137Cys
ENST00000085219.9:c.410C>G ENSP00000085219.4:p.Ser137Cys
ENST00000270311.10:c.410C>G ENSP00000270311.7:p.Ser137Cys
ENST00000341773.10:c.410C>G ENSP00000339349.6:p.Ser137Cys
ENST00000419549.6:c.7C>G ENSP00000403822.2:p.Leu3Val
ENST00000536635.6:c.410C>G ENSP00000442279.1:p.Ser137Cys
ENST00000544992.6:c.410C>G ENSP00000441237.1:p.Ser137Cys
ENST00000593867.5:c.410C>G ENSP00000471972.1:p.Ser137Cys
ENST00000594250.5:c.410C>G ENSP00000469984.1:p.Ser137Cys
ENST00000594349.1:c.377C>G ENSP00000470724.1:p.Ser126Cys
ENST00000595419.5:n.614C>G
ENST00000596492.5:n.948C>G
ENST00000597433.1:n.428C>G
ENST00000597916.5:c.404C>G ENSP00000472762.1:p.Ser135Cys
ENST00000598028.5:n.45-3114C>G
ENST00000598138.5:n.440C>G
ENST00000598815.5:n.44+3692C>G
ENST00000599717.5:c.*262C>G ENSP00000470681.1:n.*262C>G
ENST00000599811.5:c.410C>G ENSP00000469523.1:p.Ser137Cys
ENST00000600131.5:c.404C>G ENSP00000469503.1:p.Ser135Cys
ENST00000600424.5:c.404C>G ENSP00000471399.1:p.Ser135Cys
ENST00000600655.1:n.36+3692C>G
ENST00000600905.5:n.373C>G
ENST00000601329.5:n.43+3692C>G
ENST00000601414.5:n.430C>G
ENST00000601732.5:n.314C>G
ENST00000601769.5:c.404C>G ENSP00000470193.1:p.Ser135Cys
ENST00000602224.5:n.414C>G
NM_001185099.1:c.410C>G NP_001172028.1:p.Ser137Cys
NM_001185100.1:c.410C>G NP_001172029.1:p.Ser137Cys
NM_001185101.1:c.410C>G NP_001172030.1:p.Ser137Cys
NM_001278417.1:c.7C>G NP_001265346.1:p.Leu3Val
NM_001771.3:c.410C>G NP_001762.2:p.Ser137Cys
NM_001771.4:c.410C>G MANE Select NP_001762.2:p.Ser137Cys
NM_001185099.2:c.410C>G NP_001172028.1:p.Ser137Cys
NM_001185100.2:c.410C>G NP_001172029.1:p.Ser137Cys
NM_001278417.2:c.7C>G NP_001265346.1:p.Leu3Val
NM_001185101.2:c.410C>G NP_001172030.1:p.Ser137Cys