Canonical Allele Identifier: CA2739969099

Gene: BLK

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11564430T>G , CM000670.2:g.11564430T>G	GRCh38
NC_000008.10:g.11421939T>G , CM000670.1:g.11421939T>G	GRCh37
NC_000008.9:g.11459348T>G	NCBI36
NG_023543.1:g.75419T>G
NG_023543.2:g.75419T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.1948T>G
ENST00000696154.1:c.*1158T>G	ENSP00000512445.1:n.*1158T>G
ENST00000259089.9:c.*322T>G MANE Select	ENSP00000259089.4:n.*322T>G
ENST00000645242.1:c.*322T>G	ENSP00000494690.1:n.*322T>G
ENST00000259089.8:c.*322T>G	ENSP00000259089.4:n.*322T>G
ENST00000526097.1:n.1780T>G
ENST00000529894.1:c.*322T>G	ENSP00000433663.1:n.*322T>G
NM_001715.2:c.*322T>G	NP_001706.2:n.*322T>G
XM_011543824.1:c.*322T>G	XP_011542126.1:n.*322T>G
XM_011543825.1:c.*322T>G	XP_011542127.1:n.*322T>G
XM_011543826.1:c.*322T>G	XP_011542128.1:n.*322T>G
XM_011543827.1:c.*322T>G	XP_011542129.1:n.*322T>G
NM_001330465.1:c.*322T>G	NP_001317394.1:n.*322T>G
XM_011543825.3:c.*322T>G	XP_011542127.1:n.*322T>G
NM_001715.3:c.*322T>G MANE Select	NP_001706.2:n.*322T>G
NM_001330465.2:c.*322T>G	NP_001317394.1:n.*322T>G