Canonical Allele Identifier: CA459320816

Gene: BLK

Linked Data

• MyVariant Identifiers: chr8:g.11421476C>A (hg19)

Genomic Alleles

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

Transcript Alleles

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