Canonical Allele Identifier: CA2526783296

Gene: CD19

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28937353del , CM000678.2:g.28937353del	GRCh38
NC_000016.9:g.28948674del , CM000678.1:g.28948674del	GRCh37
NC_000016.8:g.28856175del	NCBI36
NG_007275.1:g.10415del , LRG_35:g.10415del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324662.8:c.1281del	ENSP00000313419.4:p.Gln429ArgfsTer?
ENST00000538922.8:c.1281del MANE Select	ENSP00000437940.2:p.Gln429ArgfsTer?
ENST00000324662.7:c.1281del	ENSP00000313419.3:p.Gln429ArgfsTer?
ENST00000538922.5:c.1281del	ENSP00000437940.1:p.Gln429ArgfsTer?
ENST00000565089.5:n.1615del
ENST00000567368.1:n.421del
ENST00000567541.5:c.1281del	ENSP00000456201.1:p.Gln429ArgfsTer?
ENST00000611258.4:c.1280del	ENSP00000481090.1:p.Leu427TrpfsTer16
NM_001178098.1:c.1281del	NP_001171569.1:p.Gln429ArgfsTer?
NM_001770.5:c.1281del , LRG_35t1:c.1281del	NP_001761.3:p.Gln429ArgfsTer?
XM_006721103.2:c.1014del	XP_006721166.1:p.Gln340ArgfsTer?
XM_006721103.3:c.1014del	XP_006721166.1:p.Gln340ArgfsTer?
XM_017023893.1:c.1014del	XP_016879382.1:p.Gln340ArgfsTer?
NM_001178098.2:c.1281del	NP_001171569.1:p.Gln429ArgfsTer?
NM_001770.6:c.1281del MANE Select	NP_001761.3:p.Gln429ArgfsTer?
NM_001385732.1:c.1014del	NP_001372661.1:p.Gln340ArgfsTer?
NR_169755.1:n.1623del