Canonical Allele Identifier: CA1763909874

Gene: BLK

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11502129G= , CM000670.2:g.11502129G=	GRCh38
NC_000008.10:g.11359638G= , CM000670.1:g.11359638G=	GRCh37
NC_000008.9:g.11397047G=	NCBI36
NG_023543.1:g.13118G=
NG_023543.2:g.13118G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001715.3:c.-2+7538G= MANE Select	NP_001706.2:n.-2+7538G=
ENST00000259089.9:c.-2+7538G= MANE Select	ENSP00000259089.4:n.-2+7538G=
NM_001330465.1:c.-91+7538G=	NP_001317394.1:n.-91+7538G=
NM_001330465.2:c.-91+7538G=	NP_001317394.1:n.-91+7538G=
NM_001715.2:c.-2+7538G=	NP_001706.2:n.-2+7538G=
ENST00000259089.8:c.-2+7538G=	ENSP00000259089.4:n.-2+7538G=
ENST00000525389.1:n.424-7021G=
ENST00000529894.1:c.-91+7538G=	ENSP00000433663.1:n.-91+7538G=
ENST00000645242.1:c.-91+14962G=	ENSP00000494690.1:n.-91+14962G=
ENST00000696154.1:c.-91+14962G=	ENSP00000512445.1:n.-91+14962G=
ENST00000696154.2:n.274+14962G=
XM_011543824.1:c.-2+7538G=	XP_011542126.1:n.-2+7538G=
XM_011543827.1:c.-91+7538G=	XP_011542129.1:n.-91+7538G=
XM_011543828.1:c.-2+7538G=	XP_011542130.1:n.-2+7538G=
XM_011543828.3:c.-2+7538G=	XP_011542130.1:n.-2+7538G=
XM_011543829.1:c.-2+7538G=	XP_011542131.1:n.-2+7538G=
XM_011543829.3:c.-2+7538G=	XP_011542131.1:n.-2+7538G=