Canonical Allele Identifier: CA1763963719

Gene: BLK

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11564043T= , CM000670.2:g.11564043T=	GRCh38
NC_000008.10:g.11421552T= , CM000670.1:g.11421552T=	GRCh37
NC_000008.9:g.11458961T=	NCBI36
NG_023543.1:g.75032T=
NG_023543.2:g.75032T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.1561T=
ENST00000696154.1:c.*771T=	ENSP00000512445.1:n.*771T=
ENST00000696155.1:n.337T=
ENST00000259089.9:c.1453T= MANE Select	ENSP00000259089.4:p.Phe485=
ENST00000645242.1:c.1240T=	ENSP00000494690.1:p.Phe414=
ENST00000259089.8:c.1453T=	ENSP00000259089.4:p.Phe485=
ENST00000526097.1:n.1393T=
ENST00000529894.1:c.1240T=	ENSP00000433663.1:p.Phe414=
NM_001715.2:c.1453T=	NP_001706.2:p.Phe485=
XM_011543824.1:c.1531T=	XP_011542126.1:p.Phe511=
XM_011543825.1:c.1531T=	XP_011542127.1:p.Phe511=
XM_011543826.1:c.1531T=	XP_011542128.1:p.Phe511=
XM_011543827.1:c.1318T=	XP_011542129.1:p.Phe440=
NM_001330465.1:c.1240T=	NP_001317394.1:p.Phe414=
XM_011543825.3:c.1531T=	XP_011542127.1:p.Phe511=
NM_001715.3:c.1453T= MANE Select	NP_001706.2:p.Phe485=
NM_001330465.2:c.1240T=	NP_001317394.1:p.Phe414=