Canonical Allele Identifier: CA405331979

Gene: CD22

Linked Data

• gnomAD v4: 19-35332924-G-C
• MyVariant Identifiers: chr19:g.35823827G>C (hg19) ; chr19:g.35332924G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35332924G>C , CM000681.2:g.35332924G>C	GRCh38
NC_000019.9:g.35823827G>C , CM000681.1:g.35823827G>C	GRCh37
NC_000019.8:g.40515667G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000085219.10:c.412G>C MANE Select	ENSP00000085219.4:p.Glu138Gln
ENST00000085219.9:c.412G>C	ENSP00000085219.4:p.Glu138Gln
ENST00000270311.10:c.412G>C	ENSP00000270311.7:p.Glu138Gln
ENST00000341773.10:c.412G>C	ENSP00000339349.6:p.Glu138Gln
ENST00000419549.6:c.9G>C	ENSP00000403822.2:p.Leu3=
ENST00000536635.6:c.412G>C	ENSP00000442279.1:p.Glu138Gln
ENST00000544992.6:c.412G>C	ENSP00000441237.1:p.Glu138Gln
ENST00000593867.5:c.412G>C	ENSP00000471972.1:p.Glu138Gln
ENST00000594250.5:c.412G>C	ENSP00000469984.1:p.Glu138Gln
ENST00000594349.1:c.379G>C	ENSP00000470724.1:p.Val127Leu
ENST00000595419.5:n.616G>C
ENST00000596492.5:n.950G>C
ENST00000597433.1:n.430G>C
ENST00000597916.5:c.406G>C	ENSP00000472762.1:p.Glu136Gln
ENST00000598028.5:n.45-3112G>C
ENST00000598138.5:n.442G>C
ENST00000598815.5:n.44+3694G>C
ENST00000599717.5:c.*264G>C	ENSP00000470681.1:n.*264G>C
ENST00000599811.5:c.412G>C	ENSP00000469523.1:p.Asp138His
ENST00000600131.5:c.406G>C	ENSP00000469503.1:p.Glu136Gln
ENST00000600424.5:c.406G>C	ENSP00000471399.1:p.Asp136His
ENST00000600655.1:n.36+3694G>C
ENST00000600905.5:n.375G>C
ENST00000601329.5:n.43+3694G>C
ENST00000601414.5:n.432G>C
ENST00000601732.5:n.316G>C
ENST00000601769.5:c.406G>C	ENSP00000470193.1:p.Val136Leu
ENST00000602224.5:n.416G>C
NM_001185099.1:c.412G>C	NP_001172028.1:p.Glu138Gln
NM_001185100.1:c.412G>C	NP_001172029.1:p.Glu138Gln
NM_001185101.1:c.412G>C	NP_001172030.1:p.Glu138Gln
NM_001278417.1:c.9G>C	NP_001265346.1:p.Leu3=
NM_001771.3:c.412G>C	NP_001762.2:p.Glu138Gln
NM_001771.4:c.412G>C MANE Select	NP_001762.2:p.Glu138Gln
NM_001185099.2:c.412G>C	NP_001172028.1:p.Glu138Gln
NM_001185100.2:c.412G>C	NP_001172029.1:p.Glu138Gln
NM_001278417.2:c.9G>C	NP_001265346.1:p.Leu3=
NM_001185101.2:c.412G>C	NP_001172030.1:p.Glu138Gln