Canonical Allele Identifier: CA2739969149

Gene: BLK

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11564496A>C , CM000670.2:g.11564496A>C	GRCh38
NC_000008.10:g.11422005A>C , CM000670.1:g.11422005A>C	GRCh37
NC_000008.9:g.11459414A>C	NCBI36
NG_023543.1:g.75485A>C
NG_023543.2:g.75485A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.2014A>C
ENST00000696154.1:c.*1224A>C	ENSP00000512445.1:n.*1224A>C
ENST00000259089.9:c.*388A>C MANE Select	ENSP00000259089.4:n.*388A>C
ENST00000645242.1:c.*388A>C	ENSP00000494690.1:n.*388A>C
ENST00000259089.8:c.*388A>C	ENSP00000259089.4:n.*388A>C
ENST00000526097.1:n.1846A>C
ENST00000529894.1:c.*388A>C	ENSP00000433663.1:n.*388A>C
NM_001715.2:c.*388A>C	NP_001706.2:n.*388A>C
XM_011543824.1:c.*388A>C	XP_011542126.1:n.*388A>C
XM_011543825.1:c.*388A>C	XP_011542127.1:n.*388A>C
XM_011543826.1:c.*388A>C	XP_011542128.1:n.*388A>C
XM_011543827.1:c.*388A>C	XP_011542129.1:n.*388A>C
NM_001330465.1:c.*388A>C	NP_001317394.1:n.*388A>C
XM_011543825.3:c.*388A>C	XP_011542127.1:n.*388A>C
NM_001715.3:c.*388A>C MANE Select	NP_001706.2:n.*388A>C
NM_001330465.2:c.*388A>C	NP_001317394.1:n.*388A>C