Canonical Allele Identifier: CA370316904

Gene: BLK

Linked Data

• gnomAD v4: 8-11564025-G-T
• MyVariant Identifiers: chr8:g.11421534G>T (hg19) ; chr8:g.11564025G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11564025G>T , CM000670.2:g.11564025G>T	GRCh38
NC_000008.10:g.11421534G>T , CM000670.1:g.11421534G>T	GRCh37
NC_000008.9:g.11458943G>T	NCBI36
NG_023543.1:g.75014G>T
NG_023543.2:g.75014G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.1543G>T
ENST00000696154.1:c.*753G>T	ENSP00000512445.1:n.*753G>T
ENST00000696155.1:n.319G>T
ENST00000259089.9:c.1435G>T MANE Select	ENSP00000259089.4:p.Glu479Ter
ENST00000645242.1:c.1222G>T	ENSP00000494690.1:p.Glu408Ter
ENST00000259089.8:c.1435G>T	ENSP00000259089.4:p.Glu479Ter
ENST00000526097.1:n.1375G>T
ENST00000529894.1:c.1222G>T	ENSP00000433663.1:p.Glu408Ter
NM_001715.2:c.1435G>T	NP_001706.2:p.Glu479Ter
XM_011543824.1:c.1513G>T	XP_011542126.1:p.Glu505Ter
XM_011543825.1:c.1513G>T	XP_011542127.1:p.Glu505Ter
XM_011543826.1:c.1513G>T	XP_011542128.1:p.Glu505Ter
XM_011543827.1:c.1300G>T	XP_011542129.1:p.Glu434Ter
NM_001330465.1:c.1222G>T	NP_001317394.1:p.Glu408Ter
XM_011543825.3:c.1513G>T	XP_011542127.1:p.Glu505Ter
NM_001715.3:c.1435G>T MANE Select	NP_001706.2:p.Glu479Ter
NM_001330465.2:c.1222G>T	NP_001317394.1:p.Glu408Ter