Canonical Allele Identifier: CA2526257298

Gene: BLK

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11564017_11564020del , CM000670.2:g.11564017_11564020del	GRCh38
NC_000008.10:g.11421526_11421529del , CM000670.1:g.11421526_11421529del	GRCh37
NC_000008.9:g.11458935_11458938del	NCBI36
NG_023543.1:g.75006_75009del
NG_023543.2:g.75006_75009del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.1535_1538del
ENST00000696154.1:c.*745_*748del	ENSP00000512445.1:n.*745_*748del
ENST00000696155.1:n.311_314del
ENST00000259089.9:c.1427_1430del MANE Select	ENSP00000259089.4:p.Arg476ProfsTer?
ENST00000645242.1:c.1214_1217del	ENSP00000494690.1:p.Arg405ProfsTer?
ENST00000259089.8:c.1427_1430del	ENSP00000259089.4:p.Arg476ProfsTer?
ENST00000526097.1:n.1367_1370del
ENST00000529894.1:c.1214_1217del	ENSP00000433663.1:p.Arg405ProfsTer?
NM_001715.2:c.1427_1430del	NP_001706.2:p.Arg476ProfsTer?
XM_011543824.1:c.1505_1508del	XP_011542126.1:p.Arg502ProfsTer?
XM_011543825.1:c.1505_1508del	XP_011542127.1:p.Arg502ProfsTer?
XM_011543826.1:c.1505_1508del	XP_011542128.1:p.Arg502ProfsTer?
XM_011543827.1:c.1292_1295del	XP_011542129.1:p.Arg431ProfsTer?
NM_001330465.1:c.1214_1217del	NP_001317394.1:p.Arg405ProfsTer?
XM_011543825.3:c.1505_1508del	XP_011542127.1:p.Arg502ProfsTer?
NM_001715.3:c.1427_1430del MANE Select	NP_001706.2:p.Arg476ProfsTer?
NM_001330465.2:c.1214_1217del	NP_001317394.1:p.Arg405ProfsTer?