Canonical Allele Identifier: CA2215894855

Gene: CD19

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28937705_28937706delinsCA , CM000678.2:g.28937705_28937706delinsCA	GRCh38
NC_000016.9:g.28949026_28949027delinsCA , CM000678.1:g.28949026_28949027delinsCA	GRCh37
NC_000016.8:g.28856527_28856528delinsCA	NCBI36
NG_007275.1:g.10767_10768delinsCA , LRG_35:g.10767_10768delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324662.8:c.1429+25_1429+26delinsCA	ENSP00000313419.4:n.1429+25_1429+26delinsCA
ENST00000538922.8:c.1429+25_1429+26delinsCA MANE Select	ENSP00000437940.2:n.1429+25_1429+26delinsCA
ENST00000324662.7:c.1429+25_1429+26delinsCA	ENSP00000313419.3:n.1429+25_1429+26delinsCA
ENST00000538922.5:c.1429+25_1429+26delinsCA	ENSP00000437940.1:n.1429+25_1429+26delinsCA
ENST00000565089.5:n.1863+25_1863+26delinsCA
ENST00000567368.1:n.569+25_569+26delinsCA
ENST00000567541.5:c.1429+25_1429+26delinsCA	ENSP00000456201.1:n.1429+25_1429+26delinsCA
ENST00000611258.4:c.*24+25_*24+26delinsCA	ENSP00000481090.1:n.*24+25_*24+26delinsCA
NM_001178098.1:c.1429+25_1429+26delinsCA	NP_001171569.1:n.1429+25_1429+26delinsCA
NM_001770.5:c.1429+25_1429+26delinsCA , LRG_35t1:c.1429+25_1429+26delinsCA	NP_001761.3:n.1429+25_1429+26delinsCA
XM_006721103.2:c.1162+25_1162+26delinsCA	XP_006721166.1:n.1162+25_1162+26delinsCA
XM_006721103.3:c.1162+25_1162+26delinsCA	XP_006721166.1:n.1162+25_1162+26delinsCA
XM_017023893.1:c.1162+25_1162+26delinsCA	XP_016879382.1:n.1162+25_1162+26delinsCA
NM_001178098.2:c.1429+25_1429+26delinsCA	NP_001171569.1:n.1429+25_1429+26delinsCA
NM_001770.6:c.1429+25_1429+26delinsCA MANE Select	NP_001761.3:n.1429+25_1429+26delinsCA
NM_001385732.1:c.1162+25_1162+26delinsCA	NP_001372661.1:n.1162+25_1162+26delinsCA
NR_169755.1:n.1771+25_1771+26delinsCA