Canonical Allele Identifier: CA645586400
Gene: CD19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28937056del , CM000678.2:g.28937056del GRCh38
NC_000016.9:g.28948377del , CM000678.1:g.28948377del GRCh37
NC_000016.8:g.28855878del NCBI36
NG_007275.1:g.10118del , LRG_35:g.10118del

Transcript Alleles

HGVS Amino-acid Change
ENST00000324662.8:c.1118del ENSP00000313419.4:p.Gly373AlafsTer?
ENST00000538922.8:c.1118del MANE Select ENSP00000437940.2:p.Gly373AlafsTer?
ENST00000324662.7:c.1118del ENSP00000313419.3:p.Gly373AlafsTer?
ENST00000538922.5:c.1118del ENSP00000437940.1:p.Gly373AlafsTer?
ENST00000565089.5:n.1452del
ENST00000567368.1:n.258del
ENST00000567541.5:c.1118del ENSP00000456201.1:p.Gly373AlafsTer?
ENST00000611258.4:c.1118del ENSP00000481090.1:p.Gly373AlafsTer?
NM_001178098.1:c.1118del NP_001171569.1:p.Gly373AlafsTer?
NM_001770.5:c.1118del , LRG_35t1:c.1118del NP_001761.3:p.Gly373AlafsTer?
XM_006721103.2:c.851del XP_006721166.1:p.Gly284AlafsTer?
XR_950871.1:n.1131del
XR_950872.1:n.1020del
XM_006721103.3:c.851del XP_006721166.1:p.Gly284AlafsTer?
XM_017023893.1:c.851del XP_016879382.1:p.Gly284AlafsTer?
XR_950871.2:n.1114del
NM_001178098.2:c.1118del NP_001171569.1:p.Gly373AlafsTer?
NM_001770.6:c.1118del MANE Select NP_001761.3:p.Gly373AlafsTer?
NM_001385732.1:c.851del NP_001372661.1:p.Gly284AlafsTer?
NR_169755.1:n.1460del