Canonical Allele Identifier: CA920100394

Gene: CD22

Linked Data

• dbSNP Id: rs1599673074

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35333058_35333060del , CM000681.2:g.35333058_35333060del	GRCh38
NC_000019.9:g.35823961_35823963del , CM000681.1:g.35823961_35823963del	GRCh37
NC_000019.8:g.40515801_40515803del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000085219.10:c.412+134_412+136del MANE Select	ENSP00000085219.4:n.412+134_412+136del
ENST00000085219.9:c.412+134_412+136del	ENSP00000085219.4:n.412+134_412+136del
ENST00000270311.10:c.412+134_412+136del	ENSP00000270311.7:n.412+134_412+136del
ENST00000341773.10:c.412+134_412+136del	ENSP00000339349.6:n.412+134_412+136del
ENST00000419549.6:c.9+134_9+136del	ENSP00000403822.2:n.9+134_9+136del
ENST00000536635.6:c.412+134_412+136del	ENSP00000442279.1:n.412+134_412+136del
ENST00000544992.6:c.412+134_412+136del	ENSP00000441237.1:n.412+134_412+136del
ENST00000593867.5:c.412+134_412+136del	ENSP00000471972.1:n.412+134_412+136del
ENST00000594250.5:c.412+134_412+136del	ENSP00000469984.1:n.412+134_412+136del
ENST00000594349.1:c.379+134_379+136del	ENSP00000470724.1:n.379+134_379+136del
ENST00000596492.5:n.950+134_950+136del
ENST00000597433.1:n.430+134_430+136del
ENST00000597916.5:c.406+134_406+136del	ENSP00000472762.1:n.406+134_406+136del
ENST00000598028.5:n.45-2978_45-2976del
ENST00000598138.5:n.442+134_442+136del
ENST00000598815.5:n.44+3828_44+3830del
ENST00000599717.5:c.*264+134_*264+136del	ENSP00000470681.1:n.*264+134_*264+136del
ENST00000599811.5:c.412+134_412+136del	ENSP00000469523.1:n.412+134_412+136del
ENST00000600131.5:c.406+134_406+136del	ENSP00000469503.1:n.406+134_406+136del
ENST00000600424.5:c.406+134_406+136del	ENSP00000471399.1:n.406+134_406+136del
ENST00000600655.1:n.36+3828_36+3830del
ENST00000600905.5:n.375+134_375+136del
ENST00000601329.5:n.43+3828_43+3830del
ENST00000601414.5:n.432+134_432+136del
ENST00000601732.5:n.316+134_316+136del
ENST00000601769.5:c.406+134_406+136del	ENSP00000470193.1:n.406+134_406+136del
ENST00000602224.5:n.550_552del
NM_001185099.1:c.412+134_412+136del	NP_001172028.1:n.412+134_412+136del
NM_001185100.1:c.412+134_412+136del	NP_001172029.1:n.412+134_412+136del
NM_001185101.1:c.412+134_412+136del	NP_001172030.1:n.412+134_412+136del
NM_001278417.1:c.9+134_9+136del	NP_001265346.1:n.9+134_9+136del
NM_001771.3:c.412+134_412+136del	NP_001762.2:n.412+134_412+136del
NM_001771.4:c.412+134_412+136del MANE Select	NP_001762.2:n.412+134_412+136del
NM_001185099.2:c.412+134_412+136del	NP_001172028.1:n.412+134_412+136del
NM_001185100.2:c.412+134_412+136del	NP_001172029.1:n.412+134_412+136del
NM_001278417.2:c.9+134_9+136del	NP_001265346.1:n.9+134_9+136del
NM_001185101.2:c.412+134_412+136del	NP_001172030.1:n.412+134_412+136del