Canonical Allele Identifier: CA4629658

Gene: BLK

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11543317A>G , CM000670.2:g.11543317A>G	GRCh38
NC_000008.10:g.11400826A>G , CM000670.1:g.11400826A>G	GRCh37
NC_000008.9:g.11438235A>G	NCBI36
NG_023543.1:g.54306A>G
NG_023543.2:g.54306A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001715.3:c.93A>G MANE Select	NP_001706.2:p.Gln31=
ENST00000259089.9:c.93A>G MANE Select	ENSP00000259089.4:p.Gln31=
NM_001330465.1:c.-90-2735A>G	NP_001317394.1:n.-90-2735A>G
NM_001330465.2:c.-90-2735A>G	NP_001317394.1:n.-90-2735A>G
NM_001715.2:c.93A>G	NP_001706.2:p.Gln31=
ENST00000259089.8:c.93A>G	ENSP00000259089.4:p.Gln31=
ENST00000529894.1:c.-90-2735A>G	ENSP00000433663.1:n.-90-2735A>G
ENST00000645242.1:c.-90-2735A>G	ENSP00000494690.1:n.-90-2735A>G
ENST00000696154.1:c.-90-2735A>G	ENSP00000512445.1:n.-90-2735A>G
ENST00000696154.2:n.275-2735A>G
XM_011543824.1:c.93A>G	XP_011542126.1:p.Gln31=
XM_011543825.1:c.93A>G	XP_011542127.1:p.Gln31=
XM_011543825.3:c.93A>G	XP_011542127.1:p.Gln31=
XM_011543826.1:c.93A>G	XP_011542128.1:p.Gln31=
XM_011543827.1:c.-90-2735A>G	XP_011542129.1:n.-90-2735A>G
XM_011543828.1:c.93A>G	XP_011542130.1:p.Gln31=
XM_011543828.3:c.93A>G	XP_011542130.1:p.Gln31=
XM_011543829.1:c.93A>G	XP_011542131.1:p.Gln31=
XM_011543829.3:c.93A>G	XP_011542131.1:p.Gln31=