Canonical Allele Identifier: CA1763963611

Gene: BLK

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11563967C= , CM000670.2:g.11563967C=	GRCh38
NC_000008.10:g.11421476C= , CM000670.1:g.11421476C=	GRCh37
NC_000008.9:g.11458885C=	NCBI36
NG_023543.1:g.74956C=
NG_023543.2:g.74956C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.1485C=
ENST00000696154.1:c.*695C=	ENSP00000512445.1:n.*695C=
ENST00000696155.1:n.261C=
ENST00000259089.9:c.1377C= MANE Select	ENSP00000259089.4:p.Thr459=
ENST00000645242.1:c.1164C=	ENSP00000494690.1:p.Thr388=
ENST00000259089.8:c.1377C=	ENSP00000259089.4:p.Thr459=
ENST00000526097.1:n.1317C=
ENST00000529894.1:c.1164C=	ENSP00000433663.1:p.Thr388=
NM_001715.2:c.1377C=	NP_001706.2:p.Thr459=
XM_011543824.1:c.1455C=	XP_011542126.1:p.Thr485=
XM_011543825.1:c.1455C=	XP_011542127.1:p.Thr485=
XM_011543826.1:c.1455C=	XP_011542128.1:p.Thr485=
XM_011543827.1:c.1242C=	XP_011542129.1:p.Thr414=
NM_001330465.1:c.1164C=	NP_001317394.1:p.Thr388=
XM_011543825.3:c.1455C=	XP_011542127.1:p.Thr485=
NM_001715.3:c.1377C= MANE Select	NP_001706.2:p.Thr459=
NM_001330465.2:c.1164C=	NP_001317394.1:p.Thr388=