Canonical Allele Identifier: CA1763963603

Gene: BLK

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11563964C= , CM000670.2:g.11563964C=	GRCh38
NC_000008.10:g.11421473C= , CM000670.1:g.11421473C=	GRCh37
NC_000008.9:g.11458882C=	NCBI36
NG_023543.1:g.74953C=
NG_023543.2:g.74953C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.1482C=
ENST00000696154.1:c.*692C=	ENSP00000512445.1:n.*692C=
ENST00000696155.1:n.258C=
ENST00000259089.9:c.1374C= MANE Select	ENSP00000259089.4:p.Asp458=
ENST00000645242.1:c.1161C=	ENSP00000494690.1:p.Asp387=
ENST00000259089.8:c.1374C=	ENSP00000259089.4:p.Asp458=
ENST00000526097.1:n.1314C=
ENST00000529894.1:c.1161C=	ENSP00000433663.1:p.Asp387=
NM_001715.2:c.1374C=	NP_001706.2:p.Asp458=
XM_011543824.1:c.1452C=	XP_011542126.1:p.Asp484=
XM_011543825.1:c.1452C=	XP_011542127.1:p.Asp484=
XM_011543826.1:c.1452C=	XP_011542128.1:p.Asp484=
XM_011543827.1:c.1239C=	XP_011542129.1:p.Asp413=
NM_001330465.1:c.1161C=	NP_001317394.1:p.Asp387=
XM_011543825.3:c.1452C=	XP_011542127.1:p.Asp484=
NM_001715.3:c.1374C= MANE Select	NP_001706.2:p.Asp458=
NM_001330465.2:c.1161C=	NP_001317394.1:p.Asp387=