Canonical Allele Identifier: CA1763964513

Gene: BLK

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11564554C= , CM000670.2:g.11564554C=	GRCh38
NC_000008.10:g.11422063C= , CM000670.1:g.11422063C=	GRCh37
NC_000008.9:g.11459472C=	NCBI36
NG_023543.1:g.75543C=
NG_023543.2:g.75543C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.2072C=
ENST00000696154.1:c.*1282C=	ENSP00000512445.1:n.*1282C=
ENST00000259089.9:c.*446C= MANE Select	ENSP00000259089.4:n.*446C=
ENST00000645242.1:c.*446C=	ENSP00000494690.1:n.*446C=
ENST00000259089.8:c.*446C=	ENSP00000259089.4:n.*446C=
ENST00000526097.1:n.1904C=
NM_001715.2:c.*446C=	NP_001706.2:n.*446C=
XM_011543824.1:c.*446C=	XP_011542126.1:n.*446C=
XM_011543825.1:c.*446C=	XP_011542127.1:n.*446C=
XM_011543826.1:c.*446C=	XP_011542128.1:n.*446C=
XM_011543827.1:c.*446C=	XP_011542129.1:n.*446C=
NM_001330465.1:c.*446C=	NP_001317394.1:n.*446C=
XM_011543825.3:c.*446C=	XP_011542127.1:n.*446C=
NM_001715.3:c.*446C= MANE Select	NP_001706.2:n.*446C=
NM_001330465.2:c.*446C=	NP_001317394.1:n.*446C=