Canonical Allele Identifier: CA2632552994

Gene: CD19

Linked Data

• gnomAD v4: 16-28937207-TGGACTGGGC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28937208_28937216del , CM000678.2:g.28937208_28937216del	GRCh38
NC_000016.9:g.28948529_28948537del , CM000678.1:g.28948529_28948537del	GRCh37
NC_000016.8:g.28856030_28856038del	NCBI36
NG_007275.1:g.10270_10278del , LRG_35:g.10270_10278del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324662.8:c.1199-63_1199-55del	ENSP00000313419.4:n.1199-63_1199-55del
ENST00000538922.8:c.1199-63_1199-55del MANE Select	ENSP00000437940.2:n.1199-63_1199-55del
ENST00000324662.7:c.1199-63_1199-55del	ENSP00000313419.3:n.1199-63_1199-55del
ENST00000538922.5:c.1199-63_1199-55del	ENSP00000437940.1:n.1199-63_1199-55del
ENST00000565089.5:n.1533-63_1533-55del
ENST00000567368.1:n.339-63_339-55del
ENST00000567541.5:c.1199-63_1199-55del	ENSP00000456201.1:n.1199-63_1199-55del
ENST00000611258.4:c.1198-63_1198-55del	ENSP00000481090.1:n.1198-63_1198-55del
NM_001178098.1:c.1199-63_1199-55del	NP_001171569.1:n.1199-63_1199-55del
NM_001770.5:c.1199-63_1199-55del , LRG_35t1:c.1199-63_1199-55del	NP_001761.3:n.1199-63_1199-55del
XM_006721103.2:c.932-63_932-55del	XP_006721166.1:n.932-63_932-55del
XM_006721103.3:c.932-63_932-55del	XP_006721166.1:n.932-63_932-55del
XM_017023893.1:c.932-63_932-55del	XP_016879382.1:n.932-63_932-55del
NM_001178098.2:c.1199-63_1199-55del	NP_001171569.1:n.1199-63_1199-55del
NM_001770.6:c.1199-63_1199-55del MANE Select	NP_001761.3:n.1199-63_1199-55del
NM_001385732.1:c.932-63_932-55del	NP_001372661.1:n.932-63_932-55del
NR_169755.1:n.1541-63_1541-55del