Canonical Allele Identifier: CA2215894588

Gene: CD19

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28937173_28937174delinsTG , CM000678.2:g.28937173_28937174delinsTG	GRCh38
NC_000016.9:g.28948494_28948495delinsTG , CM000678.1:g.28948494_28948495delinsTG	GRCh37
NC_000016.8:g.28855995_28855996delinsTG	NCBI36
NG_007275.1:g.10235_10236delinsTG , LRG_35:g.10235_10236delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324662.8:c.1198+37_1198+38delinsTG	ENSP00000313419.4:n.1198+37_1198+38delinsTG
ENST00000538922.8:c.1198+37_1198+38delinsTG MANE Select	ENSP00000437940.2:n.1198+37_1198+38delinsTG
ENST00000324662.7:c.1198+37_1198+38delinsTG	ENSP00000313419.3:n.1198+37_1198+38delinsTG
ENST00000538922.5:c.1198+37_1198+38delinsTG	ENSP00000437940.1:n.1198+37_1198+38delinsTG
ENST00000565089.5:n.1532+37_1532+38delinsTG
ENST00000567368.1:n.338+37_338+38delinsTG
ENST00000567541.5:c.1198+37_1198+38delinsTG	ENSP00000456201.1:n.1198+37_1198+38delinsTG
ENST00000611258.4:c.1197+37_1197+38delinsTG	ENSP00000481090.1:n.1197+37_1197+38delinsTG
NM_001178098.1:c.1198+37_1198+38delinsTG	NP_001171569.1:n.1198+37_1198+38delinsTG
NM_001770.5:c.1198+37_1198+38delinsTG , LRG_35t1:c.1198+37_1198+38delinsTG	NP_001761.3:n.1198+37_1198+38delinsTG
XM_006721103.2:c.931+37_931+38delinsTG	XP_006721166.1:n.931+37_931+38delinsTG
XM_006721103.3:c.931+37_931+38delinsTG	XP_006721166.1:n.931+37_931+38delinsTG
XM_017023893.1:c.931+37_931+38delinsTG	XP_016879382.1:n.931+37_931+38delinsTG
NM_001178098.2:c.1198+37_1198+38delinsTG	NP_001171569.1:n.1198+37_1198+38delinsTG
NM_001770.6:c.1198+37_1198+38delinsTG MANE Select	NP_001761.3:n.1198+37_1198+38delinsTG
NM_001385732.1:c.931+37_931+38delinsTG	NP_001372661.1:n.931+37_931+38delinsTG
NR_169755.1:n.1540+37_1540+38delinsTG