Canonical Allele Identifier: CA370316906

Gene: BLK

Linked Data

• MyVariant Identifiers: chr8:g.11421535A>T (hg19) ; chr8:g.11564026A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11564026A>T , CM000670.2:g.11564026A>T	GRCh38
NC_000008.10:g.11421535A>T , CM000670.1:g.11421535A>T	GRCh37
NC_000008.9:g.11458944A>T	NCBI36
NG_023543.1:g.75015A>T
NG_023543.2:g.75015A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.1544A>T
ENST00000696154.1:c.*754A>T	ENSP00000512445.1:n.*754A>T
ENST00000696155.1:n.320A>T
ENST00000259089.9:c.1436A>T MANE Select	ENSP00000259089.4:p.Glu479Val
ENST00000645242.1:c.1223A>T	ENSP00000494690.1:p.Glu408Val
ENST00000259089.8:c.1436A>T	ENSP00000259089.4:p.Glu479Val
ENST00000526097.1:n.1376A>T
ENST00000529894.1:c.1223A>T	ENSP00000433663.1:p.Glu408Val
NM_001715.2:c.1436A>T	NP_001706.2:p.Glu479Val
XM_011543824.1:c.1514A>T	XP_011542126.1:p.Glu505Val
XM_011543825.1:c.1514A>T	XP_011542127.1:p.Glu505Val
XM_011543826.1:c.1514A>T	XP_011542128.1:p.Glu505Val
XM_011543827.1:c.1301A>T	XP_011542129.1:p.Glu434Val
NM_001330465.1:c.1223A>T	NP_001317394.1:p.Glu408Val
XM_011543825.3:c.1514A>T	XP_011542127.1:p.Glu505Val
NM_001715.3:c.1436A>T MANE Select	NP_001706.2:p.Glu479Val
NM_001330465.2:c.1223A>T	NP_001317394.1:p.Glu408Val