Canonical Allele Identifier: CA2686158479
Gene: BLK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11564105del , CM000670.2:g.11564105del GRCh38
NC_000008.10:g.11421614del , CM000670.1:g.11421614del GRCh37
NC_000008.9:g.11459023del NCBI36
NG_023543.1:g.75094del
NG_023543.2:g.75094del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696154.2:n.1623del
ENST00000696154.1:c.*833del ENSP00000512445.1:n.*833del
ENST00000696155.1:n.399del
ENST00000259089.9:c.1515del MANE Select ENSP00000259089.4:p.Ter506SerextTer?
ENST00000645242.1:c.1302del ENSP00000494690.1:p.Ter435SerextTer?
ENST00000259089.8:c.1515del ENSP00000259089.4:p.Ter506SerextTer?
ENST00000526097.1:n.1455del
ENST00000529894.1:c.1302del ENSP00000433663.1:p.Ter435SerextTer?
NM_001715.2:c.1515del NP_001706.2:p.Ter506SerextTer?
XM_011543824.1:c.1593del XP_011542126.1:p.Ter532SerextTer?
XM_011543825.1:c.1593del XP_011542127.1:p.Ter532SerextTer?
XM_011543826.1:c.1593del XP_011542128.1:p.Ter532SerextTer?
XM_011543827.1:c.1380del XP_011542129.1:p.Ter461SerextTer?
NM_001330465.1:c.1302del NP_001317394.1:p.Ter435SerextTer?
XM_011543825.3:c.1593del XP_011542127.1:p.Ter532SerextTer?
NM_001715.3:c.1515del MANE Select NP_001706.2:p.Ter506SerextTer?
NM_001330465.2:c.1302del NP_001317394.1:p.Ter435SerextTer?