Canonical Allele Identifier: CA370316846

Gene: BLK

Linked Data

• MyVariant Identifiers: chr8:g.11421516T>G (hg19) ; chr8:g.11564007T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11564007T>G , CM000670.2:g.11564007T>G	GRCh38
NC_000008.10:g.11421516T>G , CM000670.1:g.11421516T>G	GRCh37
NC_000008.9:g.11458925T>G	NCBI36
NG_023543.1:g.74996T>G
NG_023543.2:g.74996T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.1525T>G
ENST00000696154.1:c.*735T>G	ENSP00000512445.1:n.*735T>G
ENST00000696155.1:n.301T>G
ENST00000259089.9:c.1417T>G MANE Select	ENSP00000259089.4:p.Trp473Gly
ENST00000645242.1:c.1204T>G	ENSP00000494690.1:p.Trp402Gly
ENST00000259089.8:c.1417T>G	ENSP00000259089.4:p.Trp473Gly
ENST00000526097.1:n.1357T>G
ENST00000529894.1:c.1204T>G	ENSP00000433663.1:p.Trp402Gly
NM_001715.2:c.1417T>G	NP_001706.2:p.Trp473Gly
XM_011543824.1:c.1495T>G	XP_011542126.1:p.Trp499Gly
XM_011543825.1:c.1495T>G	XP_011542127.1:p.Trp499Gly
XM_011543826.1:c.1495T>G	XP_011542128.1:p.Trp499Gly
XM_011543827.1:c.1282T>G	XP_011542129.1:p.Trp428Gly
NM_001330465.1:c.1204T>G	NP_001317394.1:p.Trp402Gly
XM_011543825.3:c.1495T>G	XP_011542127.1:p.Trp499Gly
NM_001715.3:c.1417T>G MANE Select	NP_001706.2:p.Trp473Gly
NM_001330465.2:c.1204T>G	NP_001317394.1:p.Trp402Gly