Canonical Allele Identifier: CA1763963723

Gene: BLK

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11564046C= , CM000670.2:g.11564046C=	GRCh38
NC_000008.10:g.11421555C= , CM000670.1:g.11421555C=	GRCh37
NC_000008.9:g.11458964C=	NCBI36
NG_023543.1:g.75035C=
NG_023543.2:g.75035C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.1564C=
ENST00000696154.1:c.*774C=	ENSP00000512445.1:n.*774C=
ENST00000696155.1:n.340C=
ENST00000259089.9:c.1456C= MANE Select	ENSP00000259089.4:p.Leu486=
ENST00000645242.1:c.1243C=	ENSP00000494690.1:p.Leu415=
ENST00000259089.8:c.1456C=	ENSP00000259089.4:p.Leu486=
ENST00000526097.1:n.1396C=
ENST00000529894.1:c.1243C=	ENSP00000433663.1:p.Leu415=
NM_001715.2:c.1456C=	NP_001706.2:p.Leu486=
XM_011543824.1:c.1534C=	XP_011542126.1:p.Leu512=
XM_011543825.1:c.1534C=	XP_011542127.1:p.Leu512=
XM_011543826.1:c.1534C=	XP_011542128.1:p.Leu512=
XM_011543827.1:c.1321C=	XP_011542129.1:p.Leu441=
NM_001330465.1:c.1243C=	NP_001317394.1:p.Leu415=
XM_011543825.3:c.1534C=	XP_011542127.1:p.Leu512=
NM_001715.3:c.1456C= MANE Select	NP_001706.2:p.Leu486=
NM_001330465.2:c.1243C=	NP_001317394.1:p.Leu415=