Canonical Allele Identifier: CA2739969226

Gene: BLK

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11564571T>G , CM000670.2:g.11564571T>G	GRCh38
NC_000008.10:g.11422080T>G , CM000670.1:g.11422080T>G	GRCh37
NC_000008.9:g.11459489T>G	NCBI36
NG_023543.1:g.75560T>G
NG_023543.2:g.75560T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.2089T>G
ENST00000696154.1:c.*1299T>G	ENSP00000512445.1:n.*1299T>G
ENST00000259089.9:c.*463T>G MANE Select	ENSP00000259089.4:n.*463T>G
ENST00000645242.1:c.*463T>G	ENSP00000494690.1:n.*463T>G
ENST00000259089.8:c.*463T>G	ENSP00000259089.4:n.*463T>G
ENST00000526097.1:n.1921T>G
NM_001715.2:c.*463T>G	NP_001706.2:n.*463T>G
XM_011543824.1:c.*463T>G	XP_011542126.1:n.*463T>G
XM_011543825.1:c.*463T>G	XP_011542127.1:n.*463T>G
XM_011543826.1:c.*463T>G	XP_011542128.1:n.*463T>G
XM_011543827.1:c.*463T>G	XP_011542129.1:n.*463T>G
NM_001330465.1:c.*463T>G	NP_001317394.1:n.*463T>G
XM_011543825.3:c.*463T>G	XP_011542127.1:n.*463T>G
NM_001715.3:c.*463T>G MANE Select	NP_001706.2:n.*463T>G
NM_001330465.2:c.*463T>G	NP_001317394.1:n.*463T>G