Canonical Allele Identifier: CA2686153742
Gene: BLK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11548208_11548209insGGGTCAGCCA , CM000670.2:g.11548208_11548209insGGGTCAGCCA GRCh38
NC_000008.10:g.11405717_11405718insGGGTCAGCCA , CM000670.1:g.11405717_11405718insGGGTCAGCCA GRCh37
NC_000008.9:g.11443126_11443127insGGGTCAGCCA NCBI36
NG_023543.1:g.59197_59198insGGGTCAGCCA
NG_023543.2:g.59197_59198insGGGTCAGCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000696154.2:n.420+83_420+84insGGGTCAGCCA
ENST00000696154.1:c.56+83_56+84insGGGTCAGCCA ENSP00000512445.1:n.56+83_56+84insGGGTCAGCCA
ENST00000259089.9:c.269+83_269+84insGGGTCAGCCA MANE Select ENSP00000259089.4:n.269+83_269+84insGGGTCAGCCA
ENST00000645242.1:c.56+83_56+84insGGGTCAGCCA ENSP00000494690.1:n.56+83_56+84insGGGTCAGCCA
ENST00000259089.8:c.269+83_269+84insGGGTCAGCCA ENSP00000259089.4:n.269+83_269+84insGGGTCAGCCA
ENST00000529894.1:c.56+83_56+84insGGGTCAGCCA ENSP00000433663.1:n.56+83_56+84insGGGTCAGCCA
ENST00000533828.1:n.467+83_467+84insGGGTCAGCCA
NM_001715.2:c.269+83_269+84insGGGTCAGCCA NP_001706.2:n.269+83_269+84insGGGTCAGCCA
XM_011543824.1:c.269+83_269+84insGGGTCAGCCA XP_011542126.1:n.269+83_269+84insGGGTCAGCCA
XM_011543825.1:c.269+83_269+84insGGGTCAGCCA XP_011542127.1:n.269+83_269+84insGGGTCAGCCA
XM_011543826.1:c.269+83_269+84insGGGTCAGCCA XP_011542128.1:n.269+83_269+84insGGGTCAGCCA
XM_011543827.1:c.56+83_56+84insGGGTCAGCCA XP_011542129.1:n.56+83_56+84insGGGTCAGCCA
XM_011543828.1:c.269+83_269+84insGGGTCAGCCA XP_011542130.1:n.269+83_269+84insGGGTCAGCCA
XM_011543829.1:c.269+83_269+84insGGGTCAGCCA XP_011542131.1:n.269+83_269+84insGGGTCAGCCA
NM_001330465.1:c.56+83_56+84insGGGTCAGCCA NP_001317394.1:n.56+83_56+84insGGGTCAGCCA
XM_011543825.3:c.269+83_269+84insGGGTCAGCCA XP_011542127.1:n.269+83_269+84insGGGTCAGCCA
XM_011543828.3:c.269+83_269+84insGGGTCAGCCA XP_011542130.1:n.269+83_269+84insGGGTCAGCCA
XM_011543829.3:c.269+83_269+84insGGGTCAGCCA XP_011542131.1:n.269+83_269+84insGGGTCAGCCA
NM_001715.3:c.269+83_269+84insGGGTCAGCCA MANE Select NP_001706.2:n.269+83_269+84insGGGTCAGCCA
NM_001330465.2:c.56+83_56+84insGGGTCAGCCA NP_001317394.1:n.56+83_56+84insGGGTCAGCCA