Canonical Allele Identifier: CA370316802

Gene: BLK

Linked Data

• gnomAD v4: 8-11563995-A-G
• MyVariant Identifiers: chr8:g.11421504A>G (hg19) ; chr8:g.11563995A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11563995A>G , CM000670.2:g.11563995A>G	GRCh38
NC_000008.10:g.11421504A>G , CM000670.1:g.11421504A>G	GRCh37
NC_000008.9:g.11458913A>G	NCBI36
NG_023543.1:g.74984A>G
NG_023543.2:g.74984A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.1513A>G
ENST00000696154.1:c.*723A>G	ENSP00000512445.1:n.*723A>G
ENST00000696155.1:n.289A>G
ENST00000259089.9:c.1405A>G MANE Select	ENSP00000259089.4:p.Ile469Val
ENST00000645242.1:c.1192A>G	ENSP00000494690.1:p.Ile398Val
ENST00000259089.8:c.1405A>G	ENSP00000259089.4:p.Ile469Val
ENST00000526097.1:n.1345A>G
ENST00000529894.1:c.1192A>G	ENSP00000433663.1:p.Ile398Val
NM_001715.2:c.1405A>G	NP_001706.2:p.Ile469Val
XM_011543824.1:c.1483A>G	XP_011542126.1:p.Ile495Val
XM_011543825.1:c.1483A>G	XP_011542127.1:p.Ile495Val
XM_011543826.1:c.1483A>G	XP_011542128.1:p.Ile495Val
XM_011543827.1:c.1270A>G	XP_011542129.1:p.Ile424Val
NM_001330465.1:c.1192A>G	NP_001317394.1:p.Ile398Val
XM_011543825.3:c.1483A>G	XP_011542127.1:p.Ile495Val
NM_001715.3:c.1405A>G MANE Select	NP_001706.2:p.Ile469Val
NM_001330465.2:c.1192A>G	NP_001317394.1:p.Ile398Val