Canonical Allele Identifier: CA1763963682

Gene: BLK

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11564018G= , CM000670.2:g.11564018G=	GRCh38
NC_000008.10:g.11421527G= , CM000670.1:g.11421527G=	GRCh37
NC_000008.9:g.11458936G=	NCBI36
NG_023543.1:g.75007G=
NG_023543.2:g.75007G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.1536G=
ENST00000696154.1:c.*746G=	ENSP00000512445.1:n.*746G=
ENST00000696155.1:n.312G=
ENST00000259089.9:c.1428G= MANE Select	ENSP00000259089.4:p.Arg476=
ENST00000645242.1:c.1215G=	ENSP00000494690.1:p.Arg405=
ENST00000259089.8:c.1428G=	ENSP00000259089.4:p.Arg476=
ENST00000526097.1:n.1368G=
ENST00000529894.1:c.1215G=	ENSP00000433663.1:p.Arg405=
NM_001715.2:c.1428G=	NP_001706.2:p.Arg476=
XM_011543824.1:c.1506G=	XP_011542126.1:p.Arg502=
XM_011543825.1:c.1506G=	XP_011542127.1:p.Arg502=
XM_011543826.1:c.1506G=	XP_011542128.1:p.Arg502=
XM_011543827.1:c.1293G=	XP_011542129.1:p.Arg431=
NM_001330465.1:c.1215G=	NP_001317394.1:p.Arg405=
XM_011543825.3:c.1506G=	XP_011542127.1:p.Arg502=
NM_001715.3:c.1428G= MANE Select	NP_001706.2:p.Arg476=
NM_001330465.2:c.1215G=	NP_001317394.1:p.Arg405=