Canonical Allele Identifier: CA2686158530

Gene: BLK

Linked Data

• gnomAD v4: 8-11564153-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11564157dup , CM000670.2:g.11564157dup	GRCh38
NC_000008.10:g.11421666dup , CM000670.1:g.11421666dup	GRCh37
NC_000008.9:g.11459075dup	NCBI36
NG_023543.1:g.75146dup
NG_023543.2:g.75146dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.1675dup
ENST00000696154.1:c.*885dup	ENSP00000512445.1:n.*885dup
ENST00000696155.1:n.451dup
ENST00000259089.9:c.*49dup MANE Select	ENSP00000259089.4:n.*49dup
ENST00000645242.1:c.*49dup	ENSP00000494690.1:n.*49dup
ENST00000259089.8:c.*49dup	ENSP00000259089.4:n.*49dup
ENST00000526097.1:n.1507dup
ENST00000529894.1:c.*49dup	ENSP00000433663.1:n.*49dup
NM_001715.2:c.*49dup	NP_001706.2:n.*49dup
XM_011543824.1:c.*49dup	XP_011542126.1:n.*49dup
XM_011543825.1:c.*49dup	XP_011542127.1:n.*49dup
XM_011543826.1:c.*49dup	XP_011542128.1:n.*49dup
XM_011543827.1:c.*49dup	XP_011542129.1:n.*49dup
NM_001330465.1:c.*49dup	NP_001317394.1:n.*49dup
XM_011543825.3:c.*49dup	XP_011542127.1:n.*49dup
NM_001715.3:c.*49dup MANE Select	NP_001706.2:n.*49dup
NM_001330465.2:c.*49dup	NP_001317394.1:n.*49dup