Canonical Allele Identifier: CA1763952579
Gene: BLK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11548098A= , CM000670.2:g.11548098A= GRCh38
NC_000008.10:g.11405607A= , CM000670.1:g.11405607A= GRCh37
NC_000008.9:g.11443016A= NCBI36
NG_023543.1:g.59087A=
NG_023543.2:g.59087A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696154.2:n.393A=
ENST00000696154.1:c.29A= ENSP00000512445.1:p.Lys10=
ENST00000259089.9:c.242A= MANE Select ENSP00000259089.4:p.Lys81=
ENST00000645242.1:c.29A= ENSP00000494690.1:p.Lys10=
ENST00000259089.8:c.242A= ENSP00000259089.4:p.Lys81=
ENST00000529894.1:c.29A= ENSP00000433663.1:p.Lys10=
ENST00000533828.1:n.440A=
NM_001715.2:c.242A= NP_001706.2:p.Lys81=
XM_011543824.1:c.242A= XP_011542126.1:p.Lys81=
XM_011543825.1:c.242A= XP_011542127.1:p.Lys81=
XM_011543826.1:c.242A= XP_011542128.1:p.Lys81=
XM_011543827.1:c.29A= XP_011542129.1:p.Lys10=
XM_011543828.1:c.242A= XP_011542130.1:p.Lys81=
XM_011543829.1:c.242A= XP_011542131.1:p.Lys81=
NM_001330465.1:c.29A= NP_001317394.1:p.Lys10=
XM_011543825.3:c.242A= XP_011542127.1:p.Lys81=
XM_011543828.3:c.242A= XP_011542130.1:p.Lys81=
XM_011543829.3:c.242A= XP_011542131.1:p.Lys81=
NM_001715.3:c.242A= MANE Select NP_001706.2:p.Lys81=
NM_001330465.2:c.29A= NP_001317394.1:p.Lys10=