Canonical Allele Identifier: CA2632551867
Gene: CD19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28937018_28937019del , CM000678.2:g.28937018_28937019del GRCh38
NC_000016.9:g.28948339_28948340del , CM000678.1:g.28948339_28948340del GRCh37
NC_000016.8:g.28855840_28855841del NCBI36
NG_007275.1:g.10080_10081del , LRG_35:g.10080_10081del

Transcript Alleles

HGVS Amino-acid Change
ENST00000324662.8:c.1085-5_1085-4del ENSP00000313419.4:n.1085-5_1085-4del
ENST00000538922.8:c.1085-5_1085-4del MANE Select ENSP00000437940.2:n.1085-5_1085-4del
ENST00000324662.7:c.1085-5_1085-4del ENSP00000313419.3:n.1085-5_1085-4del
ENST00000538922.5:c.1085-5_1085-4del ENSP00000437940.1:n.1085-5_1085-4del
ENST00000565089.5:n.1419-5_1419-4del
ENST00000567368.1:n.220_221del
ENST00000567541.5:c.1085-5_1085-4del ENSP00000456201.1:n.1085-5_1085-4del
ENST00000611258.4:c.1085-5_1085-4del ENSP00000481090.1:n.1085-5_1085-4del
NM_001178098.1:c.1085-5_1085-4del NP_001171569.1:n.1085-5_1085-4del
NM_001770.5:c.1085-5_1085-4del , LRG_35t1:c.1085-5_1085-4del NP_001761.3:n.1085-5_1085-4del
XM_006721103.2:c.818-5_818-4del XP_006721166.1:n.818-5_818-4del
XR_950871.1:n.1098-5_1098-4del
XR_950872.1:n.987-5_987-4del
XM_006721103.3:c.818-5_818-4del XP_006721166.1:n.818-5_818-4del
XM_017023893.1:c.818-5_818-4del XP_016879382.1:n.818-5_818-4del
XR_950871.2:n.1081-5_1081-4del
NM_001178098.2:c.1085-5_1085-4del NP_001171569.1:n.1085-5_1085-4del
NM_001770.6:c.1085-5_1085-4del MANE Select NP_001761.3:n.1085-5_1085-4del
NM_001385732.1:c.818-5_818-4del NP_001372661.1:n.818-5_818-4del
NR_169755.1:n.1427-5_1427-4del