Canonical Allele Identifier: CA2215894630

Gene: CD19

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28937243_28937249delinsTTCCCCA , CM000678.2:g.28937243_28937249delinsTTCCCCA	GRCh38
NC_000016.9:g.28948564_28948570delinsTTCCCCA , CM000678.1:g.28948564_28948570delinsTTCCCCA	GRCh37
NC_000016.8:g.28856065_28856071delinsTTCCCCA	NCBI36
NG_007275.1:g.10305_10311delinsTTCCCCA , LRG_35:g.10305_10311delinsTTCCCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324662.8:c.1199-28_1199-22delinsTTCCCCA	ENSP00000313419.4:n.1199-28_1199-22delinsTTCCCCA
ENST00000538922.8:c.1199-28_1199-22delinsTTCCCCA MANE Select	ENSP00000437940.2:n.1199-28_1199-22delinsTTCCCCA
ENST00000324662.7:c.1199-28_1199-22delinsTTCCCCA	ENSP00000313419.3:n.1199-28_1199-22delinsTTCCCCA
ENST00000538922.5:c.1199-28_1199-22delinsTTCCCCA	ENSP00000437940.1:n.1199-28_1199-22delinsTTCCCCA
ENST00000565089.5:n.1533-28_1533-22delinsTTCCCCA
ENST00000567368.1:n.339-28_339-22delinsTTCCCCA
ENST00000567541.5:c.1199-28_1199-22delinsTTCCCCA	ENSP00000456201.1:n.1199-28_1199-22delinsTTCCCCA
ENST00000611258.4:c.1198-28_1198-22delinsTTCCCCA	ENSP00000481090.1:n.1198-28_1198-22delinsTTCCCCA
NM_001178098.1:c.1199-28_1199-22delinsTTCCCCA	NP_001171569.1:n.1199-28_1199-22delinsTTCCCCA
NM_001770.5:c.1199-28_1199-22delinsTTCCCCA , LRG_35t1:c.1199-28_1199-22delinsTTCCCCA	NP_001761.3:n.1199-28_1199-22delinsTTCCCCA
XM_006721103.2:c.932-28_932-22delinsTTCCCCA	XP_006721166.1:n.932-28_932-22delinsTTCCCCA
XM_006721103.3:c.932-28_932-22delinsTTCCCCA	XP_006721166.1:n.932-28_932-22delinsTTCCCCA
XM_017023893.1:c.932-28_932-22delinsTTCCCCA	XP_016879382.1:n.932-28_932-22delinsTTCCCCA
NM_001178098.2:c.1199-28_1199-22delinsTTCCCCA	NP_001171569.1:n.1199-28_1199-22delinsTTCCCCA
NM_001770.6:c.1199-28_1199-22delinsTTCCCCA MANE Select	NP_001761.3:n.1199-28_1199-22delinsTTCCCCA
NM_001385732.1:c.932-28_932-22delinsTTCCCCA	NP_001372661.1:n.932-28_932-22delinsTTCCCCA
NR_169755.1:n.1541-28_1541-22delinsTTCCCCA