Canonical Allele Identifier: CA2333614691

Gene: CD22 MIR5196

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35345627G= , CM000681.2:g.35345627G=	GRCh38
NC_000019.9:g.35836530G= , CM000681.1:g.35836530G=	GRCh37
NC_000019.8:g.40528370G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001771.4:c.2234G= (CD22) MANE Select	NP_001762.2:p.Gly745=
ENST00000085219.10:c.2234G= (CD22) MANE Select	ENSP00000085219.4:p.Gly745=
NM_001185099.1:c.1970G= (CD22)	NP_001172028.1:p.Gly657=
NM_001185099.2:c.1970G= (CD22)	NP_001172028.1:p.Gly657=
NM_001185100.1:c.2208+501G= (CD22)	NP_001172029.1:n.2208+501G=
NM_001185100.2:c.2208+501G= (CD22)	NP_001172029.1:n.2208+501G=
NM_001185101.1:c.1703G= (CD22)	NP_001172030.1:p.Gly568=
NM_001185101.2:c.1703G= (CD22)	NP_001172030.1:p.Gly568=
NM_001278417.1:c.1718G= (CD22)	NP_001265346.1:p.Gly573=
NM_001278417.2:c.1718G= (CD22)	NP_001265346.1:p.Gly573=
NM_001771.3:c.2234G= (CD22)	NP_001762.2:p.Gly745=
NR_049828.1:n.115G= (MIR5196)
ENST00000085219.9:c.2234G= (CD22)	ENSP00000085219.4:p.Gly745=
ENST00000270311.10:c.1703G= (CD22)	ENSP00000270311.7:p.Gly568=
ENST00000341773.10:c.1703G= (CD22)	ENSP00000339349.6:p.Gly568=
ENST00000419549.6:c.1718G= (CD22)	ENSP00000403822.2:p.Gly573=
ENST00000536635.6:c.1970G= (CD22)	ENSP00000442279.1:p.Gly657=
ENST00000544992.6:c.2208+501G= (CD22)	ENSP00000441237.1:n.2208+501G=
ENST00000594250.5:c.1703G= (CD22)	ENSP00000469984.1:p.Gly568=
ENST00000601769.5:c.*1539G= (CD22)	ENSP00000470193.1:n.*1539G=