Canonical Allele Identifier: CA2575961372

Gene: CD19

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28937858del , CM000678.2:g.28937858del	GRCh38
NC_000016.9:g.28949179del , CM000678.1:g.28949179del	GRCh37
NC_000016.8:g.28856680del	NCBI36
NG_007275.1:g.10920del , LRG_35:g.10920del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324662.8:c.1486+33del	ENSP00000313419.4:n.1486+33del
ENST00000538922.8:c.1486+33del MANE Select	ENSP00000437940.2:n.1486+33del
ENST00000324662.7:c.1486+33del	ENSP00000313419.3:n.1486+33del
ENST00000538922.5:c.1486+33del	ENSP00000437940.1:n.1486+33del
ENST00000565089.5:n.1920+33del
ENST00000567368.1:n.569+178del
ENST00000567541.5:c.1486+33del	ENSP00000456201.1:n.1486+33del
ENST00000611258.4:c.*81+33del	ENSP00000481090.1:n.*81+33del
NM_001178098.1:c.1486+33del	NP_001171569.1:n.1486+33del
NM_001770.5:c.1486+33del , LRG_35t1:c.1486+33del	NP_001761.3:n.1486+33del
XM_006721103.2:c.1219+33del	XP_006721166.1:n.1219+33del
XM_006721103.3:c.1219+33del	XP_006721166.1:n.1219+33del
XM_017023893.1:c.1219+33del	XP_016879382.1:n.1219+33del
NM_001178098.2:c.1486+33del	NP_001171569.1:n.1486+33del
NM_001770.6:c.1486+33del MANE Select	NP_001761.3:n.1486+33del
NM_001385732.1:c.1219+33del	NP_001372661.1:n.1219+33del
NR_169755.1:n.1828+33del