Canonical Allele Identifier: CA2563187167

Gene: BLK

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11563986_11563991del , CM000670.2:g.11563986_11563991del	GRCh38
NC_000008.10:g.11421495_11421500del , CM000670.1:g.11421495_11421500del	GRCh37
NC_000008.9:g.11458904_11458909del	NCBI36
NG_023543.1:g.74975_74980del
NG_023543.2:g.74975_74980del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.1504_1509del
ENST00000696154.1:c.*714_*719del	ENSP00000512445.1:n.*714_*719del
ENST00000696155.1:n.280_285del
ENST00000259089.9:c.1396_1401del MANE Select	ENSP00000259089.4:p.Arg466_Gly467del
ENST00000645242.1:c.1183_1188del	ENSP00000494690.1:p.Arg395_Gly396del
ENST00000259089.8:c.1396_1401del	ENSP00000259089.4:p.Arg466_Gly467del
ENST00000526097.1:n.1336_1341del
ENST00000529894.1:c.1183_1188del	ENSP00000433663.1:p.Arg395_Gly396del
NM_001715.2:c.1396_1401del	NP_001706.2:p.Arg466_Gly467del
XM_011543824.1:c.1474_1479del	XP_011542126.1:p.Arg492_Gly493del
XM_011543825.1:c.1474_1479del	XP_011542127.1:p.Arg492_Gly493del
XM_011543826.1:c.1474_1479del	XP_011542128.1:p.Arg492_Gly493del
XM_011543827.1:c.1261_1266del	XP_011542129.1:p.Arg421_Gly422del
NM_001330465.1:c.1183_1188del	NP_001317394.1:p.Arg395_Gly396del
XM_011543825.3:c.1474_1479del	XP_011542127.1:p.Arg492_Gly493del
NM_001715.3:c.1396_1401del MANE Select	NP_001706.2:p.Arg466_Gly467del
NM_001330465.2:c.1183_1188del	NP_001317394.1:p.Arg395_Gly396del