Canonical Allele Identifier: CA1763964429

Gene: BLK

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11564499G= , CM000670.2:g.11564499G=	GRCh38
NC_000008.10:g.11422008G= , CM000670.1:g.11422008G=	GRCh37
NC_000008.9:g.11459417G=	NCBI36
NG_023543.1:g.75488G=
NG_023543.2:g.75488G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.2017G=
ENST00000696154.1:c.*1227G=	ENSP00000512445.1:n.*1227G=
ENST00000259089.9:c.*391G= MANE Select	ENSP00000259089.4:n.*391G=
ENST00000645242.1:c.*391G=	ENSP00000494690.1:n.*391G=
ENST00000259089.8:c.*391G=	ENSP00000259089.4:n.*391G=
ENST00000526097.1:n.1849G=
ENST00000529894.1:c.*391G=	ENSP00000433663.1:n.*391G=
NM_001715.2:c.*391G=	NP_001706.2:n.*391G=
XM_011543824.1:c.*391G=	XP_011542126.1:n.*391G=
XM_011543825.1:c.*391G=	XP_011542127.1:n.*391G=
XM_011543826.1:c.*391G=	XP_011542128.1:n.*391G=
XM_011543827.1:c.*391G=	XP_011542129.1:n.*391G=
NM_001330465.1:c.*391G=	NP_001317394.1:n.*391G=
XM_011543825.3:c.*391G=	XP_011542127.1:n.*391G=
NM_001715.3:c.*391G= MANE Select	NP_001706.2:n.*391G=
NM_001330465.2:c.*391G=	NP_001317394.1:n.*391G=