Canonical Allele Identifier: CA2579093252

Gene: BLK

Linked Data

• gnomAD v4: 8-11548194-CCA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11548196_11548197del , CM000670.2:g.11548196_11548197del	GRCh38
NC_000008.10:g.11405705_11405706del , CM000670.1:g.11405705_11405706del	GRCh37
NC_000008.9:g.11443114_11443115del	NCBI36
NG_023543.1:g.59185_59186del
NG_023543.2:g.59185_59186del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.420+71_420+72del
ENST00000696154.1:c.56+71_56+72del	ENSP00000512445.1:n.56+71_56+72del
ENST00000259089.9:c.269+71_269+72del MANE Select	ENSP00000259089.4:n.269+71_269+72del
ENST00000645242.1:c.56+71_56+72del	ENSP00000494690.1:n.56+71_56+72del
ENST00000259089.8:c.269+71_269+72del	ENSP00000259089.4:n.269+71_269+72del
ENST00000529894.1:c.56+71_56+72del	ENSP00000433663.1:n.56+71_56+72del
ENST00000533828.1:n.467+71_467+72del
NM_001715.2:c.269+71_269+72del	NP_001706.2:n.269+71_269+72del
XM_011543824.1:c.269+71_269+72del	XP_011542126.1:n.269+71_269+72del
XM_011543825.1:c.269+71_269+72del	XP_011542127.1:n.269+71_269+72del
XM_011543826.1:c.269+71_269+72del	XP_011542128.1:n.269+71_269+72del
XM_011543827.1:c.56+71_56+72del	XP_011542129.1:n.56+71_56+72del
XM_011543828.1:c.269+71_269+72del	XP_011542130.1:n.269+71_269+72del
XM_011543829.1:c.269+71_269+72del	XP_011542131.1:n.269+71_269+72del
NM_001330465.1:c.56+71_56+72del	NP_001317394.1:n.56+71_56+72del
XM_011543825.3:c.269+71_269+72del	XP_011542127.1:n.269+71_269+72del
XM_011543828.3:c.269+71_269+72del	XP_011542130.1:n.269+71_269+72del
XM_011543829.3:c.269+71_269+72del	XP_011542131.1:n.269+71_269+72del
NM_001715.3:c.269+71_269+72del MANE Select	NP_001706.2:n.269+71_269+72del
NM_001330465.2:c.56+71_56+72del	NP_001317394.1:n.56+71_56+72del