Canonical Allele Identifier: CA2215894755

Gene: CD19

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28937491_28937492delinsTG , CM000678.2:g.28937491_28937492delinsTG	GRCh38
NC_000016.9:g.28948812_28948813delinsTG , CM000678.1:g.28948812_28948813delinsTG	GRCh37
NC_000016.8:g.28856313_28856314delinsTG	NCBI36
NG_007275.1:g.10553_10554delinsTG , LRG_35:g.10553_10554delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324662.8:c.1340_1341delinsTG	ENSP00000313419.4:p.Leu447=
ENST00000538922.8:c.1340_1341delinsTG MANE Select	ENSP00000437940.2:p.Leu447=
ENST00000324662.7:c.1340_1341delinsTG	ENSP00000313419.3:p.Leu447=
ENST00000538922.5:c.1340_1341delinsTG	ENSP00000437940.1:p.Leu447=
ENST00000565089.5:n.1674_1675delinsTG
ENST00000567368.1:n.480_481delinsTG
ENST00000567541.5:c.1340_1341delinsTG	ENSP00000456201.1:p.Leu447=
ENST00000611258.4:c.1339_1340delinsTG	ENSP00000481090.1:p.Trp447=
NM_001178098.1:c.1340_1341delinsTG	NP_001171569.1:p.Leu447=
NM_001770.5:c.1340_1341delinsTG , LRG_35t1:c.1340_1341delinsTG	NP_001761.3:p.Leu447=
XM_006721103.2:c.1073_1074delinsTG	XP_006721166.1:p.Leu358=
XM_006721103.3:c.1073_1074delinsTG	XP_006721166.1:p.Leu358=
XM_017023893.1:c.1073_1074delinsTG	XP_016879382.1:p.Leu358=
NM_001178098.2:c.1340_1341delinsTG	NP_001171569.1:p.Leu447=
NM_001770.6:c.1340_1341delinsTG MANE Select	NP_001761.3:p.Leu447=
NM_001385732.1:c.1073_1074delinsTG	NP_001372661.1:p.Leu358=
NR_169755.1:n.1682_1683delinsTG