Canonical Allele Identifier: CA9377052

Gene: CD22

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35344836G>A , CM000681.2:g.35344836G>A	GRCh38
NC_000019.9:g.35835739G>A , CM000681.1:g.35835739G>A	GRCh37
NC_000019.8:g.40527579G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001771.4:c.2043G>A MANE Select	NP_001762.2:p.Pro681=
ENST00000085219.10:c.2043G>A MANE Select	ENSP00000085219.4:p.Pro681=
NM_001185099.1:c.1779G>A	NP_001172028.1:p.Pro593=
NM_001185099.2:c.1779G>A	NP_001172028.1:p.Pro593=
NM_001185100.1:c.2043G>A	NP_001172029.1:p.Pro681=
NM_001185100.2:c.2043G>A	NP_001172029.1:p.Pro681=
NM_001185101.1:c.1512G>A	NP_001172030.1:p.Pro504=
NM_001185101.2:c.1512G>A	NP_001172030.1:p.Pro504=
NM_001278417.1:c.1527G>A	NP_001265346.1:p.Pro509=
NM_001278417.2:c.1527G>A	NP_001265346.1:p.Pro509=
NM_001771.3:c.2043G>A	NP_001762.2:p.Pro681=
ENST00000085219.9:c.2043G>A	ENSP00000085219.4:p.Pro681=
ENST00000270311.10:c.1512G>A	ENSP00000270311.7:p.Pro504=
ENST00000341773.10:c.1512G>A	ENSP00000339349.6:p.Pro504=
ENST00000419549.6:c.1527G>A	ENSP00000403822.2:p.Pro509=
ENST00000536635.6:c.1779G>A	ENSP00000442279.1:p.Pro593=
ENST00000544992.6:c.2043G>A	ENSP00000441237.1:p.Pro681=
ENST00000593704.1:n.106G>A
ENST00000594125.1:c.789G>A	ENSP00000473221.1:n.789G>A
ENST00000594250.5:c.1512G>A	ENSP00000469984.1:p.Pro504=
ENST00000601769.5:c.*1348G>A	ENSP00000470193.1:n.*1348G>A