Canonical Allele Identifier: CA2686158754

Gene: BLK

Linked Data

• gnomAD v4: 8-11564426-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11564426G>C , CM000670.2:g.11564426G>C	GRCh38
NC_000008.10:g.11421935G>C , CM000670.1:g.11421935G>C	GRCh37
NC_000008.9:g.11459344G>C	NCBI36
NG_023543.1:g.75415G>C
NG_023543.2:g.75415G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.1944G>C
ENST00000696154.1:c.*1154G>C	ENSP00000512445.1:n.*1154G>C
ENST00000259089.9:c.*318G>C MANE Select	ENSP00000259089.4:n.*318G>C
ENST00000645242.1:c.*318G>C	ENSP00000494690.1:n.*318G>C
ENST00000259089.8:c.*318G>C	ENSP00000259089.4:n.*318G>C
ENST00000526097.1:n.1776G>C
ENST00000529894.1:c.*318G>C	ENSP00000433663.1:n.*318G>C
NM_001715.2:c.*318G>C	NP_001706.2:n.*318G>C
XM_011543824.1:c.*318G>C	XP_011542126.1:n.*318G>C
XM_011543825.1:c.*318G>C	XP_011542127.1:n.*318G>C
XM_011543826.1:c.*318G>C	XP_011542128.1:n.*318G>C
XM_011543827.1:c.*318G>C	XP_011542129.1:n.*318G>C
NM_001330465.1:c.*318G>C	NP_001317394.1:n.*318G>C
XM_011543825.3:c.*318G>C	XP_011542127.1:n.*318G>C
NM_001715.3:c.*318G>C MANE Select	NP_001706.2:n.*318G>C
NM_001330465.2:c.*318G>C	NP_001317394.1:n.*318G>C