Canonical Allele Identifier: CA1763963662

Gene: BLK

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11564001G= , CM000670.2:g.11564001G=	GRCh38
NC_000008.10:g.11421510G= , CM000670.1:g.11421510G=	GRCh37
NC_000008.9:g.11458919G=	NCBI36
NG_023543.1:g.74990G=
NG_023543.2:g.74990G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.1519G=
ENST00000696154.1:c.*729G=	ENSP00000512445.1:n.*729G=
ENST00000696155.1:n.295G=
ENST00000259089.9:c.1411G= MANE Select	ENSP00000259089.4:p.Glu471=
ENST00000645242.1:c.1198G=	ENSP00000494690.1:p.Glu400=
ENST00000259089.8:c.1411G=	ENSP00000259089.4:p.Glu471=
ENST00000526097.1:n.1351G=
ENST00000529894.1:c.1198G=	ENSP00000433663.1:p.Glu400=
NM_001715.2:c.1411G=	NP_001706.2:p.Glu471=
XM_011543824.1:c.1489G=	XP_011542126.1:p.Glu497=
XM_011543825.1:c.1489G=	XP_011542127.1:p.Glu497=
XM_011543826.1:c.1489G=	XP_011542128.1:p.Glu497=
XM_011543827.1:c.1276G=	XP_011542129.1:p.Glu426=
NM_001330465.1:c.1198G=	NP_001317394.1:p.Glu400=
XM_011543825.3:c.1489G=	XP_011542127.1:p.Glu497=
NM_001715.3:c.1411G= MANE Select	NP_001706.2:p.Glu471=
NM_001330465.2:c.1198G=	NP_001317394.1:p.Glu400=