Canonical Allele Identifier: CA622162935

Gene: CD19

Linked Data

• dbSNP Id: rs1217553694
• gnomAD v2: 16-28948662-CG-C
• MyVariant Identifiers: chr16:g.28948663del (hg19) ; chr16:g.28937342del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28937342del , CM000678.2:g.28937342del	GRCh38
NC_000016.9:g.28948663del , CM000678.1:g.28948663del	GRCh37
NC_000016.8:g.28856164del	NCBI36
NG_007275.1:g.10404del , LRG_35:g.10404del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324662.8:c.1270del	ENSP00000313419.4:p.Asp424ThrfsTer?
ENST00000538922.8:c.1270del MANE Select	ENSP00000437940.2:p.Asp424ThrfsTer?
ENST00000324662.7:c.1270del	ENSP00000313419.3:p.Asp424ThrfsTer?
ENST00000538922.5:c.1270del	ENSP00000437940.1:p.Asp424ThrfsTer?
ENST00000565089.5:n.1604del
ENST00000567368.1:n.410del
ENST00000567541.5:c.1270del	ENSP00000456201.1:p.Asp424ThrfsTer?
ENST00000611258.4:c.1269del	ENSP00000481090.1:p.Thr424LeufsTer19
NM_001178098.1:c.1270del	NP_001171569.1:p.Asp424ThrfsTer?
NM_001770.5:c.1270del , LRG_35t1:c.1270del	NP_001761.3:p.Asp424ThrfsTer?
XM_006721103.2:c.1003del	XP_006721166.1:p.Asp335ThrfsTer?
XM_006721103.3:c.1003del	XP_006721166.1:p.Asp335ThrfsTer?
XM_017023893.1:c.1003del	XP_016879382.1:p.Asp335ThrfsTer?
NM_001178098.2:c.1270del	NP_001171569.1:p.Asp424ThrfsTer?
NM_001770.6:c.1270del MANE Select	NP_001761.3:p.Asp424ThrfsTer?
NM_001385732.1:c.1003del	NP_001372661.1:p.Asp335ThrfsTer?
NR_169755.1:n.1612del