Canonical Allele Identifier: CA2215894589

Gene: CD19

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28937174_28937176delinsGGA , CM000678.2:g.28937174_28937176delinsGGA	GRCh38
NC_000016.9:g.28948495_28948497delinsGGA , CM000678.1:g.28948495_28948497delinsGGA	GRCh37
NC_000016.8:g.28855996_28855998delinsGGA	NCBI36
NG_007275.1:g.10236_10238delinsGGA , LRG_35:g.10236_10238delinsGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324662.8:c.1198+38_1198+40delinsGGA	ENSP00000313419.4:n.1198+38_1198+40delinsGGA
ENST00000538922.8:c.1198+38_1198+40delinsGGA MANE Select	ENSP00000437940.2:n.1198+38_1198+40delinsGGA
ENST00000324662.7:c.1198+38_1198+40delinsGGA	ENSP00000313419.3:n.1198+38_1198+40delinsGGA
ENST00000538922.5:c.1198+38_1198+40delinsGGA	ENSP00000437940.1:n.1198+38_1198+40delinsGGA
ENST00000565089.5:n.1532+38_1532+40delinsGGA
ENST00000567368.1:n.338+38_338+40delinsGGA
ENST00000567541.5:c.1198+38_1198+40delinsGGA	ENSP00000456201.1:n.1198+38_1198+40delinsGGA
ENST00000611258.4:c.1197+38_1197+40delinsGGA	ENSP00000481090.1:n.1197+38_1197+40delinsGGA
NM_001178098.1:c.1198+38_1198+40delinsGGA	NP_001171569.1:n.1198+38_1198+40delinsGGA
NM_001770.5:c.1198+38_1198+40delinsGGA , LRG_35t1:c.1198+38_1198+40delinsGGA	NP_001761.3:n.1198+38_1198+40delinsGGA
XM_006721103.2:c.931+38_931+40delinsGGA	XP_006721166.1:n.931+38_931+40delinsGGA
XM_006721103.3:c.931+38_931+40delinsGGA	XP_006721166.1:n.931+38_931+40delinsGGA
XM_017023893.1:c.931+38_931+40delinsGGA	XP_016879382.1:n.931+38_931+40delinsGGA
NM_001178098.2:c.1198+38_1198+40delinsGGA	NP_001171569.1:n.1198+38_1198+40delinsGGA
NM_001770.6:c.1198+38_1198+40delinsGGA MANE Select	NP_001761.3:n.1198+38_1198+40delinsGGA
NM_001385732.1:c.931+38_931+40delinsGGA	NP_001372661.1:n.931+38_931+40delinsGGA
NR_169755.1:n.1540+38_1540+40delinsGGA