Canonical Allele Identifier: CA1763963732

Gene: BLK

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11564053C= , CM000670.2:g.11564053C=	GRCh38
NC_000008.10:g.11421562C= , CM000670.1:g.11421562C=	GRCh37
NC_000008.9:g.11458971C=	NCBI36
NG_023543.1:g.75042C=
NG_023543.2:g.75042C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.1571C=
ENST00000696154.1:c.*781C=	ENSP00000512445.1:n.*781C=
ENST00000696155.1:n.347C=
ENST00000259089.9:c.1463C= MANE Select	ENSP00000259089.4:p.Ser488=
ENST00000645242.1:c.1250C=	ENSP00000494690.1:p.Ser417=
ENST00000259089.8:c.1463C=	ENSP00000259089.4:p.Ser488=
ENST00000526097.1:n.1403C=
ENST00000529894.1:c.1250C=	ENSP00000433663.1:p.Ser417=
NM_001715.2:c.1463C=	NP_001706.2:p.Ser488=
XM_011543824.1:c.1541C=	XP_011542126.1:p.Ser514=
XM_011543825.1:c.1541C=	XP_011542127.1:p.Ser514=
XM_011543826.1:c.1541C=	XP_011542128.1:p.Ser514=
XM_011543827.1:c.1328C=	XP_011542129.1:p.Ser443=
NM_001330465.1:c.1250C=	NP_001317394.1:p.Ser417=
XM_011543825.3:c.1541C=	XP_011542127.1:p.Ser514=
NM_001715.3:c.1463C= MANE Select	NP_001706.2:p.Ser488=
NM_001330465.2:c.1250C=	NP_001317394.1:p.Ser417=