Canonical Allele Identifier: CA1763964440

Gene: BLK

Linked Data

• dbSNP Id: rs1801643523

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11564509dup , CM000670.2:g.11564509dup	GRCh38
NC_000008.10:g.11422018dup , CM000670.1:g.11422018dup	GRCh37
NC_000008.9:g.11459427dup	NCBI36
NG_023543.1:g.75498dup
NG_023543.2:g.75498dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.2027dup
ENST00000696154.1:c.*1237dup	ENSP00000512445.1:n.*1237dup
ENST00000259089.9:c.*401dup MANE Select	ENSP00000259089.4:n.*401dup
ENST00000645242.1:c.*401dup	ENSP00000494690.1:n.*401dup
ENST00000259089.8:c.*401dup	ENSP00000259089.4:n.*401dup
ENST00000526097.1:n.1859dup
ENST00000529894.1:c.*401dup	ENSP00000433663.1:n.*401dup
NM_001715.2:c.*401dup	NP_001706.2:n.*401dup
XM_011543824.1:c.*401dup	XP_011542126.1:n.*401dup
XM_011543825.1:c.*401dup	XP_011542127.1:n.*401dup
XM_011543826.1:c.*401dup	XP_011542128.1:n.*401dup
XM_011543827.1:c.*401dup	XP_011542129.1:n.*401dup
NM_001330465.1:c.*401dup	NP_001317394.1:n.*401dup
XM_011543825.3:c.*401dup	XP_011542127.1:n.*401dup
NM_001715.3:c.*401dup MANE Select	NP_001706.2:n.*401dup
NM_001330465.2:c.*401dup	NP_001317394.1:n.*401dup