Canonical Allele Identifier: CA1763963615

Gene: BLK

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11563971C= , CM000670.2:g.11563971C=	GRCh38
NC_000008.10:g.11421480C= , CM000670.1:g.11421480C=	GRCh37
NC_000008.9:g.11458889C=	NCBI36
NG_023543.1:g.74960C=
NG_023543.2:g.74960C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.1489C=
ENST00000696154.1:c.*699C=	ENSP00000512445.1:n.*699C=
ENST00000696155.1:n.265C=
ENST00000259089.9:c.1381C= MANE Select	ENSP00000259089.4:p.Pro461=
ENST00000645242.1:c.1168C=	ENSP00000494690.1:p.Pro390=
ENST00000259089.8:c.1381C=	ENSP00000259089.4:p.Pro461=
ENST00000526097.1:n.1321C=
ENST00000529894.1:c.1168C=	ENSP00000433663.1:p.Pro390=
NM_001715.2:c.1381C=	NP_001706.2:p.Pro461=
XM_011543824.1:c.1459C=	XP_011542126.1:p.Pro487=
XM_011543825.1:c.1459C=	XP_011542127.1:p.Pro487=
XM_011543826.1:c.1459C=	XP_011542128.1:p.Pro487=
XM_011543827.1:c.1246C=	XP_011542129.1:p.Pro416=
NM_001330465.1:c.1168C=	NP_001317394.1:p.Pro390=
XM_011543825.3:c.1459C=	XP_011542127.1:p.Pro487=
NM_001715.3:c.1381C= MANE Select	NP_001706.2:p.Pro461=
NM_001330465.2:c.1168C=	NP_001317394.1:p.Pro390=