Canonical Allele Identifier: CA2333608492

Gene: CD22

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35332921T= , CM000681.2:g.35332921T=	GRCh38
NC_000019.9:g.35823824T= , CM000681.1:g.35823824T=	GRCh37
NC_000019.8:g.40515664T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000085219.10:c.409T= MANE Select	ENSP00000085219.4:p.Ser137=
ENST00000085219.9:c.409T=	ENSP00000085219.4:p.Ser137=
ENST00000270311.10:c.409T=	ENSP00000270311.7:p.Ser137=
ENST00000341773.10:c.409T=	ENSP00000339349.6:p.Ser137=
ENST00000419549.6:c.6T=	ENSP00000403822.2:p.Ser2=
ENST00000536635.6:c.409T=	ENSP00000442279.1:p.Ser137=
ENST00000544992.6:c.409T=	ENSP00000441237.1:p.Ser137=
ENST00000593867.5:c.409T=	ENSP00000471972.1:p.Ser137=
ENST00000594250.5:c.409T=	ENSP00000469984.1:p.Ser137=
ENST00000594349.1:c.376T=	ENSP00000470724.1:p.Ser126=
ENST00000595419.5:n.613T=
ENST00000596492.5:n.947T=
ENST00000597433.1:n.427T=
ENST00000597916.5:c.403T=	ENSP00000472762.1:p.Ser135=
ENST00000598028.5:n.45-3115T=
ENST00000598138.5:n.439T=
ENST00000598815.5:n.44+3691T=
ENST00000599717.5:c.*261T=	ENSP00000470681.1:n.*261T=
ENST00000599811.5:c.409T=	ENSP00000469523.1:p.Ser137=
ENST00000600131.5:c.403T=	ENSP00000469503.1:p.Ser135=
ENST00000600424.5:c.403T=	ENSP00000471399.1:p.Ser135=
ENST00000600655.1:n.36+3691T=
ENST00000600905.5:n.372T=
ENST00000601329.5:n.43+3691T=
ENST00000601414.5:n.429T=
ENST00000601732.5:n.313T=
ENST00000601769.5:c.403T=	ENSP00000470193.1:p.Ser135=
ENST00000602224.5:n.413T=
NM_001185099.1:c.409T=	NP_001172028.1:p.Ser137=
NM_001185100.1:c.409T=	NP_001172029.1:p.Ser137=
NM_001185101.1:c.409T=	NP_001172030.1:p.Ser137=
NM_001278417.1:c.6T=	NP_001265346.1:p.Ser2=
NM_001771.3:c.409T=	NP_001762.2:p.Ser137=
NM_001771.4:c.409T= MANE Select	NP_001762.2:p.Ser137=
NM_001185099.2:c.409T=	NP_001172028.1:p.Ser137=
NM_001185100.2:c.409T=	NP_001172029.1:p.Ser137=
NM_001278417.2:c.6T=	NP_001265346.1:p.Ser2=
NM_001185101.2:c.409T=	NP_001172030.1:p.Ser137=