Canonical Allele Identifier: CA1763963835
Gene: BLK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11564138_11564148delinsACCTCTGCGCG , CM000670.2:g.11564138_11564148delinsACCTCTGCGCG GRCh38
NC_000008.10:g.11421647_11421657delinsACCTCTGCGCG , CM000670.1:g.11421647_11421657delinsACCTCTGCGCG GRCh37
NC_000008.9:g.11459056_11459066delinsACCTCTGCGCG NCBI36
NG_023543.1:g.75127_75137delinsACCTCTGCGCG
NG_023543.2:g.75127_75137delinsACCTCTGCGCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000696154.2:n.1656_1666delinsACCTCTGCGCG
ENST00000696154.1:c.*866_*876delinsACCTCTGCGCG ENSP00000512445.1:n.*866_*876delinsACCTCTGCGCG
ENST00000696155.1:n.432_442delinsACCTCTGCGCG
ENST00000259089.9:c.*30_*40delinsACCTCTGCGCG MANE Select ENSP00000259089.4:n.*30_*40delinsACCTCTGCGCG
ENST00000645242.1:c.*30_*40delinsACCTCTGCGCG ENSP00000494690.1:n.*30_*40delinsACCTCTGCGCG
ENST00000259089.8:c.*30_*40delinsACCTCTGCGCG ENSP00000259089.4:n.*30_*40delinsACCTCTGCGCG
ENST00000526097.1:n.1488_1498delinsACCTCTGCGCG
ENST00000529894.1:c.*30_*40delinsACCTCTGCGCG ENSP00000433663.1:n.*30_*40delinsACCTCTGCGCG
NM_001715.2:c.*30_*40delinsACCTCTGCGCG NP_001706.2:n.*30_*40delinsACCTCTGCGCG
XM_011543824.1:c.*30_*40delinsACCTCTGCGCG XP_011542126.1:n.*30_*40delinsACCTCTGCGCG
XM_011543825.1:c.*30_*40delinsACCTCTGCGCG XP_011542127.1:n.*30_*40delinsACCTCTGCGCG
XM_011543826.1:c.*30_*40delinsACCTCTGCGCG XP_011542128.1:n.*30_*40delinsACCTCTGCGCG
XM_011543827.1:c.*30_*40delinsACCTCTGCGCG XP_011542129.1:n.*30_*40delinsACCTCTGCGCG
NM_001330465.1:c.*30_*40delinsACCTCTGCGCG NP_001317394.1:n.*30_*40delinsACCTCTGCGCG
XM_011543825.3:c.*30_*40delinsACCTCTGCGCG XP_011542127.1:n.*30_*40delinsACCTCTGCGCG
NM_001715.3:c.*30_*40delinsACCTCTGCGCG MANE Select NP_001706.2:n.*30_*40delinsACCTCTGCGCG
NM_001330465.2:c.*30_*40delinsACCTCTGCGCG NP_001317394.1:n.*30_*40delinsACCTCTGCGCG