Canonical Allele Identifier: CA370317088

Gene: BLK

Linked Data

• MyVariant Identifiers: chr8:g.11421592A>T (hg19) ; chr8:g.11564083A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11564083A>T , CM000670.2:g.11564083A>T	GRCh38
NC_000008.10:g.11421592A>T , CM000670.1:g.11421592A>T	GRCh37
NC_000008.9:g.11459001A>T	NCBI36
NG_023543.1:g.75072A>T
NG_023543.2:g.75072A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.1601A>T
ENST00000696154.1:c.*811A>T	ENSP00000512445.1:n.*811A>T
ENST00000696155.1:n.377A>T
ENST00000259089.9:c.1493A>T MANE Select	ENSP00000259089.4:p.Glu498Val
ENST00000645242.1:c.1280A>T	ENSP00000494690.1:p.Glu427Val
ENST00000259089.8:c.1493A>T	ENSP00000259089.4:p.Glu498Val
ENST00000526097.1:n.1433A>T
ENST00000529894.1:c.1280A>T	ENSP00000433663.1:p.Glu427Val
NM_001715.2:c.1493A>T	NP_001706.2:p.Glu498Val
XM_011543824.1:c.1571A>T	XP_011542126.1:p.Glu524Val
XM_011543825.1:c.1571A>T	XP_011542127.1:p.Glu524Val
XM_011543826.1:c.1571A>T	XP_011542128.1:p.Glu524Val
XM_011543827.1:c.1358A>T	XP_011542129.1:p.Glu453Val
NM_001330465.1:c.1280A>T	NP_001317394.1:p.Glu427Val
XM_011543825.3:c.1571A>T	XP_011542127.1:p.Glu524Val
NM_001715.3:c.1493A>T MANE Select	NP_001706.2:p.Glu498Val
NM_001330465.2:c.1280A>T	NP_001317394.1:p.Glu427Val