Canonical Allele Identifier: CA459320868

Gene: BLK

Linked Data

• gnomAD v4: 8-11564051-G-A
• MyVariant Identifiers: chr8:g.11421560G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11564051G>A , CM000670.2:g.11564051G>A	GRCh38
NC_000008.10:g.11421560G>A , CM000670.1:g.11421560G>A	GRCh37
NC_000008.9:g.11458969G>A	NCBI36
NG_023543.1:g.75040G>A
NG_023543.2:g.75040G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.1569G>A
ENST00000696154.1:c.*779G>A	ENSP00000512445.1:n.*779G>A
ENST00000696155.1:n.345G>A
ENST00000259089.9:c.1461G>A MANE Select	ENSP00000259089.4:p.Gln487=
ENST00000645242.1:c.1248G>A	ENSP00000494690.1:p.Gln416=
ENST00000259089.8:c.1461G>A	ENSP00000259089.4:p.Gln487=
ENST00000526097.1:n.1401G>A
ENST00000529894.1:c.1248G>A	ENSP00000433663.1:p.Gln416=
NM_001715.2:c.1461G>A	NP_001706.2:p.Gln487=
XM_011543824.1:c.1539G>A	XP_011542126.1:p.Gln513=
XM_011543825.1:c.1539G>A	XP_011542127.1:p.Gln513=
XM_011543826.1:c.1539G>A	XP_011542128.1:p.Gln513=
XM_011543827.1:c.1326G>A	XP_011542129.1:p.Gln442=
NM_001330465.1:c.1248G>A	NP_001317394.1:p.Gln416=
XM_011543825.3:c.1539G>A	XP_011542127.1:p.Gln513=
NM_001715.3:c.1461G>A MANE Select	NP_001706.2:p.Gln487=
NM_001330465.2:c.1248G>A	NP_001317394.1:p.Gln416=