Canonical Allele Identifier: CA1763963877

Gene: BLK

Linked Data

• dbSNP Id: rs1801621354
• gnomAD v4: 8-11564173-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11564173C>A , CM000670.2:g.11564173C>A	GRCh38
NC_000008.10:g.11421682C>A , CM000670.1:g.11421682C>A	GRCh37
NC_000008.9:g.11459091C>A	NCBI36
NG_023543.1:g.75162C>A
NG_023543.2:g.75162C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.1691C>A
ENST00000696154.1:c.*901C>A	ENSP00000512445.1:n.*901C>A
ENST00000696155.1:n.467C>A
ENST00000259089.9:c.*65C>A MANE Select	ENSP00000259089.4:n.*65C>A
ENST00000645242.1:c.*65C>A	ENSP00000494690.1:n.*65C>A
ENST00000259089.8:c.*65C>A	ENSP00000259089.4:n.*65C>A
ENST00000526097.1:n.1523C>A
ENST00000529894.1:c.*65C>A	ENSP00000433663.1:n.*65C>A
NM_001715.2:c.*65C>A	NP_001706.2:n.*65C>A
XM_011543824.1:c.*65C>A	XP_011542126.1:n.*65C>A
XM_011543825.1:c.*65C>A	XP_011542127.1:n.*65C>A
XM_011543826.1:c.*65C>A	XP_011542128.1:n.*65C>A
XM_011543827.1:c.*65C>A	XP_011542129.1:n.*65C>A
NM_001330465.1:c.*65C>A	NP_001317394.1:n.*65C>A
XM_011543825.3:c.*65C>A	XP_011542127.1:n.*65C>A
NM_001715.3:c.*65C>A MANE Select	NP_001706.2:n.*65C>A
NM_001330465.2:c.*65C>A	NP_001317394.1:n.*65C>A