Canonical Allele Identifier: CA1763963781

Gene: BLK

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11564095A= , CM000670.2:g.11564095A=	GRCh38
NC_000008.10:g.11421604A= , CM000670.1:g.11421604A=	GRCh37
NC_000008.9:g.11459013A=	NCBI36
NG_023543.1:g.75084A=
NG_023543.2:g.75084A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.1613A=
ENST00000696154.1:c.*823A=	ENSP00000512445.1:n.*823A=
ENST00000696155.1:n.389A=
ENST00000259089.9:c.1505A= MANE Select	ENSP00000259089.4:p.Glu502=
ENST00000645242.1:c.1292A=	ENSP00000494690.1:p.Glu431=
ENST00000259089.8:c.1505A=	ENSP00000259089.4:p.Glu502=
ENST00000526097.1:n.1445A=
ENST00000529894.1:c.1292A=	ENSP00000433663.1:p.Glu431=
NM_001715.2:c.1505A=	NP_001706.2:p.Glu502=
XM_011543824.1:c.1583A=	XP_011542126.1:p.Glu528=
XM_011543825.1:c.1583A=	XP_011542127.1:p.Glu528=
XM_011543826.1:c.1583A=	XP_011542128.1:p.Glu528=
XM_011543827.1:c.1370A=	XP_011542129.1:p.Glu457=
NM_001330465.1:c.1292A=	NP_001317394.1:p.Glu431=
XM_011543825.3:c.1583A=	XP_011542127.1:p.Glu528=
NM_001715.3:c.1505A= MANE Select	NP_001706.2:p.Glu502=
NM_001330465.2:c.1292A=	NP_001317394.1:p.Glu431=