Canonical Allele Identifier: CA1763964556

Gene: BLK

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11564585G= , CM000670.2:g.11564585G=	GRCh38
NC_000008.10:g.11422094G= , CM000670.1:g.11422094G=	GRCh37
NC_000008.9:g.11459503G=	NCBI36
NG_023543.1:g.75574G=
NG_023543.2:g.75574G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.2103G=
ENST00000696154.1:c.*1313G=	ENSP00000512445.1:n.*1313G=
ENST00000259089.9:c.*477G= MANE Select	ENSP00000259089.4:n.*477G=
ENST00000645242.1:c.*477G=	ENSP00000494690.1:n.*477G=
ENST00000259089.8:c.*477G=	ENSP00000259089.4:n.*477G=
ENST00000526097.1:n.1935G=
NM_001715.2:c.*477G=	NP_001706.2:n.*477G=
XM_011543824.1:c.*477G=	XP_011542126.1:n.*477G=
XM_011543825.1:c.*477G=	XP_011542127.1:n.*477G=
XM_011543826.1:c.*477G=	XP_011542128.1:n.*477G=
XM_011543827.1:c.*477G=	XP_011542129.1:n.*477G=
NM_001330465.1:c.*477G=	NP_001317394.1:n.*477G=
XM_011543825.3:c.*477G=	XP_011542127.1:n.*477G=
NM_001715.3:c.*477G= MANE Select	NP_001706.2:n.*477G=
NM_001330465.2:c.*477G=	NP_001317394.1:n.*477G=