Canonical Allele Identifier: CA645586403

Gene: CD19

Linked Data

• dbSNP Id: rs1964809550
• gnomAD v4: 16-28937680-GGT-G
• COSMIC: COSM1377214

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28937688_28937689del , CM000678.2:g.28937688_28937689del	GRCh38
NC_000016.9:g.28949009_28949010del , CM000678.1:g.28949009_28949010del	GRCh37
NC_000016.8:g.28856510_28856511del	NCBI36
NG_007275.1:g.10750_10751del , LRG_35:g.10750_10751del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324662.8:c.1429+8_1429+9del	ENSP00000313419.4:n.1429+8_1429+9del
ENST00000538922.8:c.1429+8_1429+9del MANE Select	ENSP00000437940.2:n.1429+8_1429+9del
ENST00000324662.7:c.1429+8_1429+9del	ENSP00000313419.3:n.1429+8_1429+9del
ENST00000538922.5:c.1429+8_1429+9del	ENSP00000437940.1:n.1429+8_1429+9del
ENST00000565089.5:n.1863+8_1863+9del
ENST00000567368.1:n.569+8_569+9del
ENST00000567541.5:c.1429+8_1429+9del	ENSP00000456201.1:n.1429+8_1429+9del
ENST00000611258.4:c.*24+8_*24+9del	ENSP00000481090.1:n.*24+8_*24+9del
NM_001178098.1:c.1429+8_1429+9del	NP_001171569.1:n.1429+8_1429+9del
NM_001770.5:c.1429+8_1429+9del , LRG_35t1:c.1429+8_1429+9del	NP_001761.3:n.1429+8_1429+9del
XM_006721103.2:c.1162+8_1162+9del	XP_006721166.1:n.1162+8_1162+9del
XM_006721103.3:c.1162+8_1162+9del	XP_006721166.1:n.1162+8_1162+9del
XM_017023893.1:c.1162+8_1162+9del	XP_016879382.1:n.1162+8_1162+9del
NM_001178098.2:c.1429+8_1429+9del	NP_001171569.1:n.1429+8_1429+9del
NM_001770.6:c.1429+8_1429+9del MANE Select	NP_001761.3:n.1429+8_1429+9del
NM_001385732.1:c.1162+8_1162+9del	NP_001372661.1:n.1162+8_1162+9del
NR_169755.1:n.1771+8_1771+9del