Canonical Allele Identifier: CA1763964104

Gene: BLK

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11564330G= , CM000670.2:g.11564330G=	GRCh38
NC_000008.10:g.11421839G= , CM000670.1:g.11421839G=	GRCh37
NC_000008.9:g.11459248G=	NCBI36
NG_023543.1:g.75319G=
NG_023543.2:g.75319G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.1848G=
ENST00000696154.1:c.*1058G=	ENSP00000512445.1:n.*1058G=
ENST00000259089.9:c.*222G= MANE Select	ENSP00000259089.4:n.*222G=
ENST00000645242.1:c.*222G=	ENSP00000494690.1:n.*222G=
ENST00000259089.8:c.*222G=	ENSP00000259089.4:n.*222G=
ENST00000526097.1:n.1680G=
ENST00000529894.1:c.*222G=	ENSP00000433663.1:n.*222G=
NM_001715.2:c.*222G=	NP_001706.2:n.*222G=
XM_011543824.1:c.*222G=	XP_011542126.1:n.*222G=
XM_011543825.1:c.*222G=	XP_011542127.1:n.*222G=
XM_011543826.1:c.*222G=	XP_011542128.1:n.*222G=
XM_011543827.1:c.*222G=	XP_011542129.1:n.*222G=
NM_001330465.1:c.*222G=	NP_001317394.1:n.*222G=
XM_011543825.3:c.*222G=	XP_011542127.1:n.*222G=
NM_001715.3:c.*222G= MANE Select	NP_001706.2:n.*222G=
NM_001330465.2:c.*222G=	NP_001317394.1:n.*222G=