Canonical Allele Identifier: CA2632553017

Gene: CD19

Linked Data

• gnomAD v4: 16-28937218-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28937219dup , CM000678.2:g.28937219dup	GRCh38
NC_000016.9:g.28948540dup , CM000678.1:g.28948540dup	GRCh37
NC_000016.8:g.28856041dup	NCBI36
NG_007275.1:g.10281dup , LRG_35:g.10281dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324662.8:c.1199-52dup	ENSP00000313419.4:n.1199-52dup
ENST00000538922.8:c.1199-52dup MANE Select	ENSP00000437940.2:n.1199-52dup
ENST00000324662.7:c.1199-52dup	ENSP00000313419.3:n.1199-52dup
ENST00000538922.5:c.1199-52dup	ENSP00000437940.1:n.1199-52dup
ENST00000565089.5:n.1533-52dup
ENST00000567368.1:n.339-52dup
ENST00000567541.5:c.1199-52dup	ENSP00000456201.1:n.1199-52dup
ENST00000611258.4:c.1198-52dup	ENSP00000481090.1:n.1198-52dup
NM_001178098.1:c.1199-52dup	NP_001171569.1:n.1199-52dup
NM_001770.5:c.1199-52dup , LRG_35t1:c.1199-52dup	NP_001761.3:n.1199-52dup
XM_006721103.2:c.932-52dup	XP_006721166.1:n.932-52dup
XM_006721103.3:c.932-52dup	XP_006721166.1:n.932-52dup
XM_017023893.1:c.932-52dup	XP_016879382.1:n.932-52dup
NM_001178098.2:c.1199-52dup	NP_001171569.1:n.1199-52dup
NM_001770.6:c.1199-52dup MANE Select	NP_001761.3:n.1199-52dup
NM_001385732.1:c.932-52dup	NP_001372661.1:n.932-52dup
NR_169755.1:n.1541-52dup