Canonical Allele Identifier: CA1763952600

Gene: BLK

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11548116T= , CM000670.2:g.11548116T=	GRCh38
NC_000008.10:g.11405625T= , CM000670.1:g.11405625T=	GRCh37
NC_000008.9:g.11443034T=	NCBI36
NG_023543.1:g.59105T=
NG_023543.2:g.59105T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.411T=
ENST00000696154.1:c.47T=	ENSP00000512445.1:p.Val16=
ENST00000259089.9:c.260T= MANE Select	ENSP00000259089.4:p.Val87=
ENST00000645242.1:c.47T=	ENSP00000494690.1:p.Val16=
ENST00000259089.8:c.260T=	ENSP00000259089.4:p.Val87=
ENST00000529894.1:c.47T=	ENSP00000433663.1:p.Val16=
ENST00000533828.1:n.458T=
NM_001715.2:c.260T=	NP_001706.2:p.Val87=
XM_011543824.1:c.260T=	XP_011542126.1:p.Val87=
XM_011543825.1:c.260T=	XP_011542127.1:p.Val87=
XM_011543826.1:c.260T=	XP_011542128.1:p.Val87=
XM_011543827.1:c.47T=	XP_011542129.1:p.Val16=
XM_011543828.1:c.260T=	XP_011542130.1:p.Val87=
XM_011543829.1:c.260T=	XP_011542131.1:p.Val87=
NM_001330465.1:c.47T=	NP_001317394.1:p.Val16=
XM_011543825.3:c.260T=	XP_011542127.1:p.Val87=
XM_011543828.3:c.260T=	XP_011542130.1:p.Val87=
XM_011543829.3:c.260T=	XP_011542131.1:p.Val87=
NM_001715.3:c.260T= MANE Select	NP_001706.2:p.Val87=
NM_001330465.2:c.47T=	NP_001317394.1:p.Val16=