Canonical Allele Identifier: CA2215894967

Gene: CD19

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28937946_28937951delinsTCTCAC , CM000678.2:g.28937946_28937951delinsTCTCAC	GRCh38
NC_000016.9:g.28949267_28949272delinsTCTCAC , CM000678.1:g.28949267_28949272delinsTCTCAC	GRCh37
NC_000016.8:g.28856768_28856773delinsTCTCAC	NCBI36
NG_007275.1:g.11008_11013delinsTCTCAC , LRG_35:g.11008_11013delinsTCTCAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324662.8:c.1486+121_1486+126delinsTCTCAC	ENSP00000313419.4:n.1486+121_1486+126delinsTCTCAC
ENST00000538922.8:c.1486+121_1486+126delinsTCTCAC MANE Select	ENSP00000437940.2:n.1486+121_1486+126delinsTCTCAC
ENST00000324662.7:c.1486+121_1486+126delinsTCTCAC	ENSP00000313419.3:n.1486+121_1486+126delinsTCTCAC
ENST00000538922.5:c.1486+121_1486+126delinsTCTCAC	ENSP00000437940.1:n.1486+121_1486+126delinsTCTCAC
ENST00000565089.5:n.1920+121_1920+126delinsTCTCAC
ENST00000567368.1:n.569+266_569+271delinsTCTCAC
ENST00000567541.5:c.1486+121_1486+126delinsTCTCAC	ENSP00000456201.1:n.1486+121_1486+126delinsTCTCAC
ENST00000611258.4:c.*81+121_*81+126delinsTCTCAC	ENSP00000481090.1:n.*81+121_*81+126delinsTCTCAC
NM_001178098.1:c.1486+121_1486+126delinsTCTCAC	NP_001171569.1:n.1486+121_1486+126delinsTCTCAC
NM_001770.5:c.1486+121_1486+126delinsTCTCAC , LRG_35t1:c.1486+121_1486+126delinsTCTCAC	NP_001761.3:n.1486+121_1486+126delinsTCTCAC
XM_006721103.2:c.1219+121_1219+126delinsTCTCAC	XP_006721166.1:n.1219+121_1219+126delinsTCTCAC
XM_006721103.3:c.1219+121_1219+126delinsTCTCAC	XP_006721166.1:n.1219+121_1219+126delinsTCTCAC
XM_017023893.1:c.1219+121_1219+126delinsTCTCAC	XP_016879382.1:n.1219+121_1219+126delinsTCTCAC
NM_001178098.2:c.1486+121_1486+126delinsTCTCAC	NP_001171569.1:n.1486+121_1486+126delinsTCTCAC
NM_001770.6:c.1486+121_1486+126delinsTCTCAC MANE Select	NP_001761.3:n.1486+121_1486+126delinsTCTCAC
NM_001385732.1:c.1219+121_1219+126delinsTCTCAC	NP_001372661.1:n.1219+121_1219+126delinsTCTCAC
NR_169755.1:n.1828+121_1828+126delinsTCTCAC