Canonical Allele Identifier: CA459320862

Gene: BLK

Linked Data

• gnomAD v4: 8-11564042-G-A
• MyVariant Identifiers: chr8:g.11421551G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11564042G>A , CM000670.2:g.11564042G>A	GRCh38
NC_000008.10:g.11421551G>A , CM000670.1:g.11421551G>A	GRCh37
NC_000008.9:g.11458960G>A	NCBI36
NG_023543.1:g.75031G>A
NG_023543.2:g.75031G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.1560G>A
ENST00000696154.1:c.*770G>A	ENSP00000512445.1:n.*770G>A
ENST00000696155.1:n.336G>A
ENST00000259089.9:c.1452G>A MANE Select	ENSP00000259089.4:p.Glu484=
ENST00000645242.1:c.1239G>A	ENSP00000494690.1:p.Glu413=
ENST00000259089.8:c.1452G>A	ENSP00000259089.4:p.Glu484=
ENST00000526097.1:n.1392G>A
ENST00000529894.1:c.1239G>A	ENSP00000433663.1:p.Glu413=
NM_001715.2:c.1452G>A	NP_001706.2:p.Glu484=
XM_011543824.1:c.1530G>A	XP_011542126.1:p.Glu510=
XM_011543825.1:c.1530G>A	XP_011542127.1:p.Glu510=
XM_011543826.1:c.1530G>A	XP_011542128.1:p.Glu510=
XM_011543827.1:c.1317G>A	XP_011542129.1:p.Glu439=
NM_001330465.1:c.1239G>A	NP_001317394.1:p.Glu413=
XM_011543825.3:c.1530G>A	XP_011542127.1:p.Glu510=
NM_001715.3:c.1452G>A MANE Select	NP_001706.2:p.Glu484=
NM_001330465.2:c.1239G>A	NP_001317394.1:p.Glu413=