Canonical Allele Identifier: CA15555498
Gene: BLK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11534141A>G , CM000670.2:g.11534141A>G GRCh38
NC_000008.10:g.11391650A>G , CM000670.1:g.11391650A>G GRCh37
NC_000008.9:g.11429059A>G NCBI36
NG_023543.1:g.45130A>G
NG_023543.2:g.45130A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696154.2:n.275-11911A>G
ENST00000696154.1:c.-90-11911A>G ENSP00000512445.1:n.-90-11911A>G
ENST00000259089.9:c.-1-9083A>G MANE Select ENSP00000259089.4:n.-1-9083A>G
ENST00000645242.1:c.-90-11911A>G ENSP00000494690.1:n.-90-11911A>G
ENST00000259089.8:c.-1-9083A>G ENSP00000259089.4:n.-1-9083A>G
ENST00000529894.1:c.-90-11911A>G ENSP00000433663.1:n.-90-11911A>G
NM_001715.2:c.-1-9083A>G NP_001706.2:n.-1-9083A>G
XM_011543824.1:c.-1-9083A>G XP_011542126.1:n.-1-9083A>G
XM_011543827.1:c.-90-11911A>G XP_011542129.1:n.-90-11911A>G
XM_011543828.1:c.-1-9083A>G XP_011542130.1:n.-1-9083A>G
XM_011543829.1:c.-1-9083A>G XP_011542131.1:n.-1-9083A>G
NM_001330465.1:c.-90-11911A>G NP_001317394.1:n.-90-11911A>G
XM_011543828.3:c.-1-9083A>G XP_011542130.1:n.-1-9083A>G
XM_011543829.3:c.-1-9083A>G XP_011542131.1:n.-1-9083A>G
NM_001715.3:c.-1-9083A>G MANE Select NP_001706.2:n.-1-9083A>G
NM_001330465.2:c.-90-11911A>G NP_001317394.1:n.-90-11911A>G
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