Canonical Allele Identifier: CA2686158555

Gene: BLK

Linked Data

• gnomAD v4: 8-11564178-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11564181del , CM000670.2:g.11564181del	GRCh38
NC_000008.10:g.11421690del , CM000670.1:g.11421690del	GRCh37
NC_000008.9:g.11459099del	NCBI36
NG_023543.1:g.75170del
NG_023543.2:g.75170del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.1699del
ENST00000696154.1:c.*909del	ENSP00000512445.1:n.*909del
ENST00000696155.1:n.475del
ENST00000259089.9:c.*73del MANE Select	ENSP00000259089.4:n.*73del
ENST00000645242.1:c.*73del	ENSP00000494690.1:n.*73del
ENST00000259089.8:c.*73del	ENSP00000259089.4:n.*73del
ENST00000526097.1:n.1531del
ENST00000529894.1:c.*73del	ENSP00000433663.1:n.*73del
NM_001715.2:c.*73del	NP_001706.2:n.*73del
XM_011543824.1:c.*73del	XP_011542126.1:n.*73del
XM_011543825.1:c.*73del	XP_011542127.1:n.*73del
XM_011543826.1:c.*73del	XP_011542128.1:n.*73del
XM_011543827.1:c.*73del	XP_011542129.1:n.*73del
NM_001330465.1:c.*73del	NP_001317394.1:n.*73del
XM_011543825.3:c.*73del	XP_011542127.1:n.*73del
NM_001715.3:c.*73del MANE Select	NP_001706.2:n.*73del
NM_001330465.2:c.*73del	NP_001317394.1:n.*73del