Canonical Allele Identifier: CA1763963983

Gene: BLK

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11564266G= , CM000670.2:g.11564266G=	GRCh38
NC_000008.10:g.11421775G= , CM000670.1:g.11421775G=	GRCh37
NC_000008.9:g.11459184G=	NCBI36
NG_023543.1:g.75255G=
NG_023543.2:g.75255G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.1784G=
ENST00000696154.1:c.*994G=	ENSP00000512445.1:n.*994G=
ENST00000696155.1:n.560G=
ENST00000259089.9:c.*158G= MANE Select	ENSP00000259089.4:n.*158G=
ENST00000645242.1:c.*158G=	ENSP00000494690.1:n.*158G=
ENST00000259089.8:c.*158G=	ENSP00000259089.4:n.*158G=
ENST00000526097.1:n.1616G=
ENST00000529894.1:c.*158G=	ENSP00000433663.1:n.*158G=
NM_001715.2:c.*158G=	NP_001706.2:n.*158G=
XM_011543824.1:c.*158G=	XP_011542126.1:n.*158G=
XM_011543825.1:c.*158G=	XP_011542127.1:n.*158G=
XM_011543826.1:c.*158G=	XP_011542128.1:n.*158G=
XM_011543827.1:c.*158G=	XP_011542129.1:n.*158G=
NM_001330465.1:c.*158G=	NP_001317394.1:n.*158G=
XM_011543825.3:c.*158G=	XP_011542127.1:n.*158G=
NM_001715.3:c.*158G= MANE Select	NP_001706.2:n.*158G=
NM_001330465.2:c.*158G=	NP_001317394.1:n.*158G=