Canonical Allele Identifier: CA719707232

Gene: CD19

Linked Data

• ClinVar Variation Id: 18055
• ClinVar RCV Id: RCV000019671
• dbSNP Id: rs1393707607
• gnomAD v3: 16-28937634-TGA-T
• gnomAD v4: 16-28937634-TGA-T
• MyVariant Identifiers: chr16:g.28948956_28948957del (hg19) ; chr16:g.28937635_28937636del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28937637_28937638del , CM000678.2:g.28937637_28937638del	GRCh38
NC_000016.9:g.28948958_28948959del , CM000678.1:g.28948958_28948959del	GRCh37
NC_000016.8:g.28856459_28856460del	NCBI36
NG_007275.1:g.10699_10700del , LRG_35:g.10699_10700del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324662.8:c.1386_1387del	ENSP00000313419.4:p.Asn463ArgfsTer3
ENST00000538922.8:c.1386_1387del MANE Select	ENSP00000437940.2:p.Asn463ArgfsTer3
ENST00000324662.7:c.1386_1387del	ENSP00000313419.3:p.Asn463ArgfsTer3
ENST00000538922.5:c.1386_1387del	ENSP00000437940.1:p.Asn463ArgfsTer3
ENST00000565089.5:n.1820_1821del
ENST00000567368.1:n.526_527del
ENST00000567541.5:c.1386_1387del	ENSP00000456201.1:p.Asn463ArgfsTer3
ENST00000611258.4:c.1385_1386del	ENSP00000481090.1:p.Arg462AsnfsTer?
NM_001178098.1:c.1386_1387del	NP_001171569.1:p.Asn463ArgfsTer3
NM_001770.5:c.1386_1387del , LRG_35t1:c.1386_1387del	NP_001761.3:p.Asn463ArgfsTer3
XM_006721103.2:c.1119_1120del	XP_006721166.1:p.Asn374ArgfsTer3
XM_006721103.3:c.1119_1120del	XP_006721166.1:p.Asn374ArgfsTer3
XM_017023893.1:c.1119_1120del	XP_016879382.1:p.Asn374ArgfsTer3
NM_001178098.2:c.1386_1387del	NP_001171569.1:p.Asn463ArgfsTer3
NM_001770.6:c.1386_1387del MANE Select	NP_001761.3:p.Asn463ArgfsTer3
NM_001385732.1:c.1119_1120del	NP_001372661.1:p.Asn374ArgfsTer3
NR_169755.1:n.1728_1729del