Canonical Allele Identifier: CA370311554
Gene: BLK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11548091A>C , CM000670.2:g.11548091A>C GRCh38
NC_000008.10:g.11405600A>C , CM000670.1:g.11405600A>C GRCh37
NC_000008.9:g.11443009A>C NCBI36
NG_023543.1:g.59080A>C
NG_023543.2:g.59080A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696154.2:n.386A>C
ENST00000696154.1:c.22A>C ENSP00000512445.1:p.Met8Leu
ENST00000259089.9:c.235A>C MANE Select ENSP00000259089.4:p.Met79Leu
ENST00000645242.1:c.22A>C ENSP00000494690.1:p.Met8Leu
ENST00000259089.8:c.235A>C ENSP00000259089.4:p.Met79Leu
ENST00000529894.1:c.22A>C ENSP00000433663.1:p.Met8Leu
ENST00000533828.1:n.433A>C
NM_001715.2:c.235A>C NP_001706.2:p.Met79Leu
XM_011543824.1:c.235A>C XP_011542126.1:p.Met79Leu
XM_011543825.1:c.235A>C XP_011542127.1:p.Met79Leu
XM_011543826.1:c.235A>C XP_011542128.1:p.Met79Leu
XM_011543827.1:c.22A>C XP_011542129.1:p.Met8Leu
XM_011543828.1:c.235A>C XP_011542130.1:p.Met79Leu
XM_011543829.1:c.235A>C XP_011542131.1:p.Met79Leu
NM_001330465.1:c.22A>C NP_001317394.1:p.Met8Leu
XM_011543825.3:c.235A>C XP_011542127.1:p.Met79Leu
XM_011543828.3:c.235A>C XP_011542130.1:p.Met79Leu
XM_011543829.3:c.235A>C XP_011542131.1:p.Met79Leu
NM_001715.3:c.235A>C MANE Select NP_001706.2:p.Met79Leu
NM_001330465.2:c.22A>C NP_001317394.1:p.Met8Leu