Canonical Allele Identifier: CA1763963740

Gene: BLK

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11564058C= , CM000670.2:g.11564058C=	GRCh38
NC_000008.10:g.11421567C= , CM000670.1:g.11421567C=	GRCh37
NC_000008.9:g.11458976C=	NCBI36
NG_023543.1:g.75047C=
NG_023543.2:g.75047C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.1576C=
ENST00000696154.1:c.*786C=	ENSP00000512445.1:n.*786C=
ENST00000696155.1:n.352C=
ENST00000259089.9:c.1468C= MANE Select	ENSP00000259089.4:p.Leu490=
ENST00000645242.1:c.1255C=	ENSP00000494690.1:p.Leu419=
ENST00000259089.8:c.1468C=	ENSP00000259089.4:p.Leu490=
ENST00000526097.1:n.1408C=
ENST00000529894.1:c.1255C=	ENSP00000433663.1:p.Leu419=
NM_001715.2:c.1468C=	NP_001706.2:p.Leu490=
XM_011543824.1:c.1546C=	XP_011542126.1:p.Leu516=
XM_011543825.1:c.1546C=	XP_011542127.1:p.Leu516=
XM_011543826.1:c.1546C=	XP_011542128.1:p.Leu516=
XM_011543827.1:c.1333C=	XP_011542129.1:p.Leu445=
NM_001330465.1:c.1255C=	NP_001317394.1:p.Leu419=
XM_011543825.3:c.1546C=	XP_011542127.1:p.Leu516=
NM_001715.3:c.1468C= MANE Select	NP_001706.2:p.Leu490=
NM_001330465.2:c.1255C=	NP_001317394.1:p.Leu419=