Canonical Allele Identifier: CA1763963717

Gene: BLK

Genomic Alleles

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

Transcript Alleles

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