Canonical Allele Identifier: CA2584460208

Gene: CD22

Linked Data

• gnomAD v4: 19-35333121-CCTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35333123_35333125del , CM000681.2:g.35333123_35333125del	GRCh38
NC_000019.9:g.35824026_35824028del , CM000681.1:g.35824026_35824028del	GRCh37
NC_000019.8:g.40515866_40515868del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000085219.10:c.412+199_412+201del MANE Select	ENSP00000085219.4:n.412+199_412+201del
ENST00000085219.9:c.412+199_412+201del	ENSP00000085219.4:n.412+199_412+201del
ENST00000270311.10:c.412+199_412+201del	ENSP00000270311.7:n.412+199_412+201del
ENST00000341773.10:c.412+199_412+201del	ENSP00000339349.6:n.412+199_412+201del
ENST00000419549.6:c.9+199_9+201del	ENSP00000403822.2:n.9+199_9+201del
ENST00000536635.6:c.412+199_412+201del	ENSP00000442279.1:n.412+199_412+201del
ENST00000544992.6:c.412+199_412+201del	ENSP00000441237.1:n.412+199_412+201del
ENST00000593867.5:c.412+199_412+201del	ENSP00000471972.1:n.412+199_412+201del
ENST00000594250.5:c.412+199_412+201del	ENSP00000469984.1:n.412+199_412+201del
ENST00000594349.1:c.379+199_379+201del	ENSP00000470724.1:n.379+199_379+201del
ENST00000596492.5:n.950+199_950+201del
ENST00000597433.1:n.430+199_430+201del
ENST00000597916.5:c.406+199_406+201del	ENSP00000472762.1:n.406+199_406+201del
ENST00000598028.5:n.45-2913_45-2911del
ENST00000598138.5:n.442+199_442+201del
ENST00000598815.5:n.44+3893_44+3895del
ENST00000599717.5:c.*264+199_*264+201del	ENSP00000470681.1:n.*264+199_*264+201del
ENST00000599811.5:c.412+199_412+201del	ENSP00000469523.1:n.412+199_412+201del
ENST00000600131.5:c.406+199_406+201del	ENSP00000469503.1:n.406+199_406+201del
ENST00000600424.5:c.406+199_406+201del	ENSP00000471399.1:n.406+199_406+201del
ENST00000600655.1:n.36+3893_36+3895del
ENST00000600905.5:n.375+199_375+201del
ENST00000601329.5:n.43+3893_43+3895del
ENST00000601414.5:n.432+199_432+201del
ENST00000601732.5:n.316+199_316+201del
ENST00000601769.5:c.406+199_406+201del	ENSP00000470193.1:n.406+199_406+201del
NM_001185099.1:c.412+199_412+201del	NP_001172028.1:n.412+199_412+201del
NM_001185100.1:c.412+199_412+201del	NP_001172029.1:n.412+199_412+201del
NM_001185101.1:c.412+199_412+201del	NP_001172030.1:n.412+199_412+201del
NM_001278417.1:c.9+199_9+201del	NP_001265346.1:n.9+199_9+201del
NM_001771.3:c.412+199_412+201del	NP_001762.2:n.412+199_412+201del
NM_001771.4:c.412+199_412+201del MANE Select	NP_001762.2:n.412+199_412+201del
NM_001185099.2:c.412+199_412+201del	NP_001172028.1:n.412+199_412+201del
NM_001185100.2:c.412+199_412+201del	NP_001172029.1:n.412+199_412+201del
NM_001278417.2:c.9+199_9+201del	NP_001265346.1:n.9+199_9+201del
NM_001185101.2:c.412+199_412+201del	NP_001172030.1:n.412+199_412+201del