Canonical Allele Identifier: CA2579093514

Gene: BLK

Linked Data

• gnomAD v4: 8-11564134-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11564137del , CM000670.2:g.11564137del	GRCh38
NC_000008.10:g.11421646del , CM000670.1:g.11421646del	GRCh37
NC_000008.9:g.11459055del	NCBI36
NG_023543.1:g.75126del
NG_023543.2:g.75126del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.1655del
ENST00000696154.1:c.*865del	ENSP00000512445.1:n.*865del
ENST00000696155.1:n.431del
ENST00000259089.9:c.*29del MANE Select	ENSP00000259089.4:n.*29del
ENST00000645242.1:c.*29del	ENSP00000494690.1:n.*29del
ENST00000259089.8:c.*29del	ENSP00000259089.4:n.*29del
ENST00000526097.1:n.1487del
ENST00000529894.1:c.*29del	ENSP00000433663.1:n.*29del
NM_001715.2:c.*29del	NP_001706.2:n.*29del
XM_011543824.1:c.*29del	XP_011542126.1:n.*29del
XM_011543825.1:c.*29del	XP_011542127.1:n.*29del
XM_011543826.1:c.*29del	XP_011542128.1:n.*29del
XM_011543827.1:c.*29del	XP_011542129.1:n.*29del
NM_001330465.1:c.*29del	NP_001317394.1:n.*29del
XM_011543825.3:c.*29del	XP_011542127.1:n.*29del
NM_001715.3:c.*29del MANE Select	NP_001706.2:n.*29del
NM_001330465.2:c.*29del	NP_001317394.1:n.*29del