Canonical Allele Identifier: CA1763952591

Gene: BLK

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11548109C= , CM000670.2:g.11548109C=	GRCh38
NC_000008.10:g.11405618C= , CM000670.1:g.11405618C=	GRCh37
NC_000008.9:g.11443027C=	NCBI36
NG_023543.1:g.59098C=
NG_023543.2:g.59098C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.404C=
ENST00000696154.1:c.40C=	ENSP00000512445.1:p.Leu14=
ENST00000259089.9:c.253C= MANE Select	ENSP00000259089.4:p.Leu85=
ENST00000645242.1:c.40C=	ENSP00000494690.1:p.Leu14=
ENST00000259089.8:c.253C=	ENSP00000259089.4:p.Leu85=
ENST00000529894.1:c.40C=	ENSP00000433663.1:p.Leu14=
ENST00000533828.1:n.451C=
NM_001715.2:c.253C=	NP_001706.2:p.Leu85=
XM_011543824.1:c.253C=	XP_011542126.1:p.Leu85=
XM_011543825.1:c.253C=	XP_011542127.1:p.Leu85=
XM_011543826.1:c.253C=	XP_011542128.1:p.Leu85=
XM_011543827.1:c.40C=	XP_011542129.1:p.Leu14=
XM_011543828.1:c.253C=	XP_011542130.1:p.Leu85=
XM_011543829.1:c.253C=	XP_011542131.1:p.Leu85=
NM_001330465.1:c.40C=	NP_001317394.1:p.Leu14=
XM_011543825.3:c.253C=	XP_011542127.1:p.Leu85=
XM_011543828.3:c.253C=	XP_011542130.1:p.Leu85=
XM_011543829.3:c.253C=	XP_011542131.1:p.Leu85=
NM_001715.3:c.253C= MANE Select	NP_001706.2:p.Leu85=
NM_001330465.2:c.40C=	NP_001317394.1:p.Leu14=