Canonical Allele Identifier: CA405331977
Gene: CD22 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35332923T>A , CM000681.2:g.35332923T>A GRCh38
NC_000019.9:g.35823826T>A , CM000681.1:g.35823826T>A GRCh37
NC_000019.8:g.40515666T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000085219.10:c.411T>A MANE Select ENSP00000085219.4:p.Ser137=
ENST00000085219.9:c.411T>A ENSP00000085219.4:p.Ser137=
ENST00000270311.10:c.411T>A ENSP00000270311.7:p.Ser137=
ENST00000341773.10:c.411T>A ENSP00000339349.6:p.Ser137=
ENST00000419549.6:c.8T>A ENSP00000403822.2:p.Leu3Gln
ENST00000536635.6:c.411T>A ENSP00000442279.1:p.Ser137=
ENST00000544992.6:c.411T>A ENSP00000441237.1:p.Ser137=
ENST00000593867.5:c.411T>A ENSP00000471972.1:p.Ser137=
ENST00000594250.5:c.411T>A ENSP00000469984.1:p.Ser137=
ENST00000594349.1:c.378T>A ENSP00000470724.1:p.Ser126=
ENST00000595419.5:n.615T>A
ENST00000596492.5:n.949T>A
ENST00000597433.1:n.429T>A
ENST00000597916.5:c.405T>A ENSP00000472762.1:p.Ser135=
ENST00000598028.5:n.45-3113T>A
ENST00000598138.5:n.441T>A
ENST00000598815.5:n.44+3693T>A
ENST00000599717.5:c.*263T>A ENSP00000470681.1:n.*263T>A
ENST00000599811.5:c.411T>A ENSP00000469523.1:p.Ser137=
ENST00000600131.5:c.405T>A ENSP00000469503.1:p.Ser135=
ENST00000600424.5:c.405T>A ENSP00000471399.1:p.Ser135=
ENST00000600655.1:n.36+3693T>A
ENST00000600905.5:n.374T>A
ENST00000601329.5:n.43+3693T>A
ENST00000601414.5:n.431T>A
ENST00000601732.5:n.315T>A
ENST00000601769.5:c.405T>A ENSP00000470193.1:p.Ser135=
ENST00000602224.5:n.415T>A
NM_001185099.1:c.411T>A NP_001172028.1:p.Ser137=
NM_001185100.1:c.411T>A NP_001172029.1:p.Ser137=
NM_001185101.1:c.411T>A NP_001172030.1:p.Ser137=
NM_001278417.1:c.8T>A NP_001265346.1:p.Leu3Gln
NM_001771.3:c.411T>A NP_001762.2:p.Ser137=
NM_001771.4:c.411T>A MANE Select NP_001762.2:p.Ser137=
NM_001185099.2:c.411T>A NP_001172028.1:p.Ser137=
NM_001185100.2:c.411T>A NP_001172029.1:p.Ser137=
NM_001278417.2:c.8T>A NP_001265346.1:p.Leu3Gln
NM_001185101.2:c.411T>A NP_001172030.1:p.Ser137=