Canonical Allele Identifier: CA1763963783

Gene: BLK

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11564096G= , CM000670.2:g.11564096G=	GRCh38
NC_000008.10:g.11421605G= , CM000670.1:g.11421605G=	GRCh37
NC_000008.9:g.11459014G=	NCBI36
NG_023543.1:g.75085G=
NG_023543.2:g.75085G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.1614G=
ENST00000696154.1:c.*824G=	ENSP00000512445.1:n.*824G=
ENST00000696155.1:n.390G=
ENST00000259089.9:c.1506G= MANE Select	ENSP00000259089.4:p.Glu502=
ENST00000645242.1:c.1293G=	ENSP00000494690.1:p.Glu431=
ENST00000259089.8:c.1506G=	ENSP00000259089.4:p.Glu502=
ENST00000526097.1:n.1446G=
ENST00000529894.1:c.1293G=	ENSP00000433663.1:p.Glu431=
NM_001715.2:c.1506G=	NP_001706.2:p.Glu502=
XM_011543824.1:c.1584G=	XP_011542126.1:p.Glu528=
XM_011543825.1:c.1584G=	XP_011542127.1:p.Glu528=
XM_011543826.1:c.1584G=	XP_011542128.1:p.Glu528=
XM_011543827.1:c.1371G=	XP_011542129.1:p.Glu457=
NM_001330465.1:c.1293G=	NP_001317394.1:p.Glu431=
XM_011543825.3:c.1584G=	XP_011542127.1:p.Glu528=
NM_001715.3:c.1506G= MANE Select	NP_001706.2:p.Glu502=
NM_001330465.2:c.1293G=	NP_001317394.1:p.Glu431=