Canonical Allele Identifier: CA2563196990

Gene: CD19

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28937637_28937648del , CM000678.2:g.28937637_28937648del	GRCh38
NC_000016.9:g.28948958_28948969del , CM000678.1:g.28948958_28948969del	GRCh37
NC_000016.8:g.28856459_28856470del	NCBI36
NG_007275.1:g.10699_10710del , LRG_35:g.10699_10710del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324662.8:c.1386_1397del	ENSP00000313419.4:p.Asn463_Glu466del
ENST00000538922.8:c.1386_1397del MANE Select	ENSP00000437940.2:p.Asn463_Glu466del
ENST00000324662.7:c.1386_1397del	ENSP00000313419.3:p.Asn463_Glu466del
ENST00000538922.5:c.1386_1397del	ENSP00000437940.1:p.Asn463_Glu466del
ENST00000565089.5:n.1820_1831del
ENST00000567368.1:n.526_537del
ENST00000567541.5:c.1386_1397del	ENSP00000456201.1:p.Asn463_Glu466del
ENST00000611258.4:c.1385_1396del	ENSP00000481090.1:p.Arg462_Met465del
NM_001178098.1:c.1386_1397del	NP_001171569.1:p.Asn463_Glu466del
NM_001770.5:c.1386_1397del , LRG_35t1:c.1386_1397del	NP_001761.3:p.Asn463_Glu466del
XM_006721103.2:c.1119_1130del	XP_006721166.1:p.Asn374_Glu377del
XM_006721103.3:c.1119_1130del	XP_006721166.1:p.Asn374_Glu377del
XM_017023893.1:c.1119_1130del	XP_016879382.1:p.Asn374_Glu377del
NM_001178098.2:c.1386_1397del	NP_001171569.1:p.Asn463_Glu466del
NM_001770.6:c.1386_1397del MANE Select	NP_001761.3:p.Asn463_Glu466del
NM_001385732.1:c.1119_1130del	NP_001372661.1:p.Asn374_Glu377del
NR_169755.1:n.1728_1739del