Canonical Allele Identifier: CA405331971

Gene: CD22

Linked Data

• gnomAD v4: 19-35332920-C-T
• MyVariant Identifiers: chr19:g.35823823C>T (hg19) ; chr19:g.35332920C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35332920C>T , CM000681.2:g.35332920C>T	GRCh38
NC_000019.9:g.35823823C>T , CM000681.1:g.35823823C>T	GRCh37
NC_000019.8:g.40515663C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000085219.10:c.408C>T MANE Select	ENSP00000085219.4:p.Val136=
ENST00000085219.9:c.408C>T	ENSP00000085219.4:p.Val136=
ENST00000270311.10:c.408C>T	ENSP00000270311.7:p.Val136=
ENST00000341773.10:c.408C>T	ENSP00000339349.6:p.Val136=
ENST00000419549.6:c.5C>T	ENSP00000403822.2:p.Ser2Phe
ENST00000536635.6:c.408C>T	ENSP00000442279.1:p.Val136=
ENST00000544992.6:c.408C>T	ENSP00000441237.1:p.Val136=
ENST00000593867.5:c.408C>T	ENSP00000471972.1:p.Val136=
ENST00000594250.5:c.408C>T	ENSP00000469984.1:p.Val136=
ENST00000594349.1:c.375C>T	ENSP00000470724.1:p.Val125=
ENST00000595419.5:n.612C>T
ENST00000596492.5:n.946C>T
ENST00000597433.1:n.426C>T
ENST00000597916.5:c.402C>T	ENSP00000472762.1:p.Val134=
ENST00000598028.5:n.45-3116C>T
ENST00000598138.5:n.438C>T
ENST00000598815.5:n.44+3690C>T
ENST00000599717.5:c.*260C>T	ENSP00000470681.1:n.*260C>T
ENST00000599811.5:c.408C>T	ENSP00000469523.1:p.Val136=
ENST00000600131.5:c.402C>T	ENSP00000469503.1:p.Val134=
ENST00000600424.5:c.402C>T	ENSP00000471399.1:p.Val134=
ENST00000600655.1:n.36+3690C>T
ENST00000600905.5:n.371C>T
ENST00000601329.5:n.43+3690C>T
ENST00000601414.5:n.428C>T
ENST00000601732.5:n.312C>T
ENST00000601769.5:c.402C>T	ENSP00000470193.1:p.Val134=
ENST00000602224.5:n.412C>T
NM_001185099.1:c.408C>T	NP_001172028.1:p.Val136=
NM_001185100.1:c.408C>T	NP_001172029.1:p.Val136=
NM_001185101.1:c.408C>T	NP_001172030.1:p.Val136=
NM_001278417.1:c.5C>T	NP_001265346.1:p.Ser2Phe
NM_001771.3:c.408C>T	NP_001762.2:p.Val136=
NM_001771.4:c.408C>T MANE Select	NP_001762.2:p.Val136=
NM_001185099.2:c.408C>T	NP_001172028.1:p.Val136=
NM_001185100.2:c.408C>T	NP_001172029.1:p.Val136=
NM_001278417.2:c.5C>T	NP_001265346.1:p.Ser2Phe
NM_001185101.2:c.408C>T	NP_001172030.1:p.Val136=