Canonical Allele Identifier: CA2580797916

Gene: BLK

Genomic Alleles

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

Transcript Alleles

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