Canonical Allele Identifier: CA1763963756

Gene: BLK

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11564076G= , CM000670.2:g.11564076G=	GRCh38
NC_000008.10:g.11421585G= , CM000670.1:g.11421585G=	GRCh37
NC_000008.9:g.11458994G=	NCBI36
NG_023543.1:g.75065G=
NG_023543.2:g.75065G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.1594G=
ENST00000696154.1:c.*804G=	ENSP00000512445.1:n.*804G=
ENST00000696155.1:n.370G=
ENST00000259089.9:c.1486G= MANE Select	ENSP00000259089.4:p.Ala496=
ENST00000645242.1:c.1273G=	ENSP00000494690.1:p.Ala425=
ENST00000259089.8:c.1486G=	ENSP00000259089.4:p.Ala496=
ENST00000526097.1:n.1426G=
ENST00000529894.1:c.1273G=	ENSP00000433663.1:p.Ala425=
NM_001715.2:c.1486G=	NP_001706.2:p.Ala496=
XM_011543824.1:c.1564G=	XP_011542126.1:p.Ala522=
XM_011543825.1:c.1564G=	XP_011542127.1:p.Ala522=
XM_011543826.1:c.1564G=	XP_011542128.1:p.Ala522=
XM_011543827.1:c.1351G=	XP_011542129.1:p.Ala451=
NM_001330465.1:c.1273G=	NP_001317394.1:p.Ala425=
XM_011543825.3:c.1564G=	XP_011542127.1:p.Ala522=
NM_001715.3:c.1486G= MANE Select	NP_001706.2:p.Ala496=
NM_001330465.2:c.1273G=	NP_001317394.1:p.Ala425=