Canonical Allele Identifier: CA2686158881

Gene: BLK

Linked Data

• gnomAD v4: 8-11564551-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11564551G>T , CM000670.2:g.11564551G>T	GRCh38
NC_000008.10:g.11422060G>T , CM000670.1:g.11422060G>T	GRCh37
NC_000008.9:g.11459469G>T	NCBI36
NG_023543.1:g.75540G>T
NG_023543.2:g.75540G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.2069G>T
ENST00000696154.1:c.*1279G>T	ENSP00000512445.1:n.*1279G>T
ENST00000259089.9:c.*443G>T MANE Select	ENSP00000259089.4:n.*443G>T
ENST00000645242.1:c.*443G>T	ENSP00000494690.1:n.*443G>T
ENST00000259089.8:c.*443G>T	ENSP00000259089.4:n.*443G>T
ENST00000526097.1:n.1901G>T
NM_001715.2:c.*443G>T	NP_001706.2:n.*443G>T
XM_011543824.1:c.*443G>T	XP_011542126.1:n.*443G>T
XM_011543825.1:c.*443G>T	XP_011542127.1:n.*443G>T
XM_011543826.1:c.*443G>T	XP_011542128.1:n.*443G>T
XM_011543827.1:c.*443G>T	XP_011542129.1:n.*443G>T
NM_001330465.1:c.*443G>T	NP_001317394.1:n.*443G>T
XM_011543825.3:c.*443G>T	XP_011542127.1:n.*443G>T
NM_001715.3:c.*443G>T MANE Select	NP_001706.2:n.*443G>T
NM_001330465.2:c.*443G>T	NP_001317394.1:n.*443G>T