Canonical Allele Identifier: CA2215894591

Gene: CD19

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28937176_28937177delinsAG , CM000678.2:g.28937176_28937177delinsAG	GRCh38
NC_000016.9:g.28948497_28948498delinsAG , CM000678.1:g.28948497_28948498delinsAG	GRCh37
NC_000016.8:g.28855998_28855999delinsAG	NCBI36
NG_007275.1:g.10238_10239delinsAG , LRG_35:g.10238_10239delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324662.8:c.1198+40_1198+41delinsAG	ENSP00000313419.4:n.1198+40_1198+41delinsAG
ENST00000538922.8:c.1198+40_1198+41delinsAG MANE Select	ENSP00000437940.2:n.1198+40_1198+41delinsAG
ENST00000324662.7:c.1198+40_1198+41delinsAG	ENSP00000313419.3:n.1198+40_1198+41delinsAG
ENST00000538922.5:c.1198+40_1198+41delinsAG	ENSP00000437940.1:n.1198+40_1198+41delinsAG
ENST00000565089.5:n.1532+40_1532+41delinsAG
ENST00000567368.1:n.338+40_338+41delinsAG
ENST00000567541.5:c.1198+40_1198+41delinsAG	ENSP00000456201.1:n.1198+40_1198+41delinsAG
ENST00000611258.4:c.1197+40_1197+41delinsAG	ENSP00000481090.1:n.1197+40_1197+41delinsAG
NM_001178098.1:c.1198+40_1198+41delinsAG	NP_001171569.1:n.1198+40_1198+41delinsAG
NM_001770.5:c.1198+40_1198+41delinsAG , LRG_35t1:c.1198+40_1198+41delinsAG	NP_001761.3:n.1198+40_1198+41delinsAG
XM_006721103.2:c.931+40_931+41delinsAG	XP_006721166.1:n.931+40_931+41delinsAG
XM_006721103.3:c.931+40_931+41delinsAG	XP_006721166.1:n.931+40_931+41delinsAG
XM_017023893.1:c.931+40_931+41delinsAG	XP_016879382.1:n.931+40_931+41delinsAG
NM_001178098.2:c.1198+40_1198+41delinsAG	NP_001171569.1:n.1198+40_1198+41delinsAG
NM_001770.6:c.1198+40_1198+41delinsAG MANE Select	NP_001761.3:n.1198+40_1198+41delinsAG
NM_001385732.1:c.931+40_931+41delinsAG	NP_001372661.1:n.931+40_931+41delinsAG
NR_169755.1:n.1540+40_1540+41delinsAG