Canonical Allele Identifier: CA1763964408
Gene: BLK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11564488_11564491delinsGCCC , CM000670.2:g.11564488_11564491delinsGCCC GRCh38
NC_000008.10:g.11421997_11422000delinsGCCC , CM000670.1:g.11421997_11422000delinsGCCC GRCh37
NC_000008.9:g.11459406_11459409delinsGCCC NCBI36
NG_023543.1:g.75477_75480delinsGCCC
NG_023543.2:g.75477_75480delinsGCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000696154.2:n.2006_2009delinsGCCC
ENST00000696154.1:c.*1216_*1219delinsGCCC ENSP00000512445.1:n.*1216_*1219delinsGCCC
ENST00000259089.9:c.*380_*383delinsGCCC MANE Select ENSP00000259089.4:n.*380_*383delinsGCCC
ENST00000645242.1:c.*380_*383delinsGCCC ENSP00000494690.1:n.*380_*383delinsGCCC
ENST00000259089.8:c.*380_*383delinsGCCC ENSP00000259089.4:n.*380_*383delinsGCCC
ENST00000526097.1:n.1838_1841delinsGCCC
ENST00000529894.1:c.*380_*383delinsGCCC ENSP00000433663.1:n.*380_*383delinsGCCC
NM_001715.2:c.*380_*383delinsGCCC NP_001706.2:n.*380_*383delinsGCCC
XM_011543824.1:c.*380_*383delinsGCCC XP_011542126.1:n.*380_*383delinsGCCC
XM_011543825.1:c.*380_*383delinsGCCC XP_011542127.1:n.*380_*383delinsGCCC
XM_011543826.1:c.*380_*383delinsGCCC XP_011542128.1:n.*380_*383delinsGCCC
XM_011543827.1:c.*380_*383delinsGCCC XP_011542129.1:n.*380_*383delinsGCCC
NM_001330465.1:c.*380_*383delinsGCCC NP_001317394.1:n.*380_*383delinsGCCC
XM_011543825.3:c.*380_*383delinsGCCC XP_011542127.1:n.*380_*383delinsGCCC
NM_001715.3:c.*380_*383delinsGCCC MANE Select NP_001706.2:n.*380_*383delinsGCCC
NM_001330465.2:c.*380_*383delinsGCCC NP_001317394.1:n.*380_*383delinsGCCC