Canonical Allele Identifier: CA2779060261

Gene: BLK

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11564591_11564594del , CM000670.2:g.11564591_11564594del	GRCh38
NC_000008.10:g.11422100_11422103del , CM000670.1:g.11422100_11422103del	GRCh37
NC_000008.9:g.11459509_11459512del	NCBI36
NG_023543.1:g.75580_75583del
NG_023543.2:g.75580_75583del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.2109_2112del
ENST00000696154.1:c.*1319_*1322del	ENSP00000512445.1:n.*1319_*1322del
ENST00000259089.9:c.*483_*486del MANE Select	ENSP00000259089.4:n.*483_*486del
ENST00000645242.1:c.*483_*486del	ENSP00000494690.1:n.*483_*486del
ENST00000259089.8:c.*483_*486del	ENSP00000259089.4:n.*483_*486del
ENST00000526097.1:n.1941_1944del
NM_001715.2:c.*483_*486del	NP_001706.2:n.*483_*486del
XM_011543824.1:c.*483_*486del	XP_011542126.1:n.*483_*486del
XM_011543825.1:c.*483_*486del	XP_011542127.1:n.*483_*486del
XM_011543826.1:c.*483_*486del	XP_011542128.1:n.*483_*486del
XM_011543827.1:c.*483_*486del	XP_011542129.1:n.*483_*486del
NM_001330465.1:c.*483_*486del	NP_001317394.1:n.*483_*486del
XM_011543825.3:c.*483_*486del	XP_011542127.1:n.*483_*486del
NM_001715.3:c.*483_*486del MANE Select	NP_001706.2:n.*483_*486del
NM_001330465.2:c.*483_*486del	NP_001317394.1:n.*483_*486del