Canonical Allele Identifier: CA1763963627

Gene: BLK

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11563976C= , CM000670.2:g.11563976C=	GRCh38
NC_000008.10:g.11421485C= , CM000670.1:g.11421485C=	GRCh37
NC_000008.9:g.11458894C=	NCBI36
NG_023543.1:g.74965C=
NG_023543.2:g.74965C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.1494C=
ENST00000696154.1:c.*704C=	ENSP00000512445.1:n.*704C=
ENST00000696155.1:n.270C=
ENST00000259089.9:c.1386C= MANE Select	ENSP00000259089.4:p.Pro462=
ENST00000645242.1:c.1173C=	ENSP00000494690.1:p.Pro391=
ENST00000259089.8:c.1386C=	ENSP00000259089.4:p.Pro462=
ENST00000526097.1:n.1326C=
ENST00000529894.1:c.1173C=	ENSP00000433663.1:p.Pro391=
NM_001715.2:c.1386C=	NP_001706.2:p.Pro462=
XM_011543824.1:c.1464C=	XP_011542126.1:p.Pro488=
XM_011543825.1:c.1464C=	XP_011542127.1:p.Pro488=
XM_011543826.1:c.1464C=	XP_011542128.1:p.Pro488=
XM_011543827.1:c.1251C=	XP_011542129.1:p.Pro417=
NM_001330465.1:c.1173C=	NP_001317394.1:p.Pro391=
XM_011543825.3:c.1464C=	XP_011542127.1:p.Pro488=
NM_001715.3:c.1386C= MANE Select	NP_001706.2:p.Pro462=
NM_001330465.2:c.1173C=	NP_001317394.1:p.Pro391=