Canonical Allele Identifier: CA1763963667

Gene: BLK

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11564010C= , CM000670.2:g.11564010C=	GRCh38
NC_000008.10:g.11421519C= , CM000670.1:g.11421519C=	GRCh37
NC_000008.9:g.11458928C=	NCBI36
NG_023543.1:g.74999C=
NG_023543.2:g.74999C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.1528C=
ENST00000696154.1:c.*738C=	ENSP00000512445.1:n.*738C=
ENST00000696155.1:n.304C=
ENST00000259089.9:c.1420C= MANE Select	ENSP00000259089.4:p.Arg474=
ENST00000645242.1:c.1207C=	ENSP00000494690.1:p.Arg403=
ENST00000259089.8:c.1420C=	ENSP00000259089.4:p.Arg474=
ENST00000526097.1:n.1360C=
ENST00000529894.1:c.1207C=	ENSP00000433663.1:p.Arg403=
NM_001715.2:c.1420C=	NP_001706.2:p.Arg474=
XM_011543824.1:c.1498C=	XP_011542126.1:p.Arg500=
XM_011543825.1:c.1498C=	XP_011542127.1:p.Arg500=
XM_011543826.1:c.1498C=	XP_011542128.1:p.Arg500=
XM_011543827.1:c.1285C=	XP_011542129.1:p.Arg429=
NM_001330465.1:c.1207C=	NP_001317394.1:p.Arg403=
XM_011543825.3:c.1498C=	XP_011542127.1:p.Arg500=
NM_001715.3:c.1420C= MANE Select	NP_001706.2:p.Arg474=
NM_001330465.2:c.1207C=	NP_001317394.1:p.Arg403=