Canonical Allele Identifier: CA459320832

Gene: BLK

Linked Data

• MyVariant Identifiers: chr8:g.11421497C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11563988C>T , CM000670.2:g.11563988C>T	GRCh38
NC_000008.10:g.11421497C>T , CM000670.1:g.11421497C>T	GRCh37
NC_000008.9:g.11458906C>T	NCBI36
NG_023543.1:g.74977C>T
NG_023543.2:g.74977C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.1506C>T
ENST00000696154.1:c.*716C>T	ENSP00000512445.1:n.*716C>T
ENST00000696155.1:n.282C>T
ENST00000259089.9:c.1398C>T MANE Select	ENSP00000259089.4:p.Arg466=
ENST00000645242.1:c.1185C>T	ENSP00000494690.1:p.Arg395=
ENST00000259089.8:c.1398C>T	ENSP00000259089.4:p.Arg466=
ENST00000526097.1:n.1338C>T
ENST00000529894.1:c.1185C>T	ENSP00000433663.1:p.Arg395=
NM_001715.2:c.1398C>T	NP_001706.2:p.Arg466=
XM_011543824.1:c.1476C>T	XP_011542126.1:p.Arg492=
XM_011543825.1:c.1476C>T	XP_011542127.1:p.Arg492=
XM_011543826.1:c.1476C>T	XP_011542128.1:p.Arg492=
XM_011543827.1:c.1263C>T	XP_011542129.1:p.Arg421=
NM_001330465.1:c.1185C>T	NP_001317394.1:p.Arg395=
XM_011543825.3:c.1476C>T	XP_011542127.1:p.Arg492=
NM_001715.3:c.1398C>T MANE Select	NP_001706.2:p.Arg466=
NM_001330465.2:c.1185C>T	NP_001317394.1:p.Arg395=