Canonical Allele Identifier: CA2686158904

Gene: BLK

Linked Data

• gnomAD v4: 8-11564570-CTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11564573_11564574del , CM000670.2:g.11564573_11564574del	GRCh38
NC_000008.10:g.11422082_11422083del , CM000670.1:g.11422082_11422083del	GRCh37
NC_000008.9:g.11459491_11459492del	NCBI36
NG_023543.1:g.75562_75563del
NG_023543.2:g.75562_75563del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.2091_2092del
ENST00000696154.1:c.*1301_*1302del	ENSP00000512445.1:n.*1301_*1302del
ENST00000259089.9:c.*465_*466del MANE Select	ENSP00000259089.4:n.*465_*466del
ENST00000645242.1:c.*465_*466del	ENSP00000494690.1:n.*465_*466del
ENST00000259089.8:c.*465_*466del	ENSP00000259089.4:n.*465_*466del
ENST00000526097.1:n.1923_1924del
NM_001715.2:c.*465_*466del	NP_001706.2:n.*465_*466del
XM_011543824.1:c.*465_*466del	XP_011542126.1:n.*465_*466del
XM_011543825.1:c.*465_*466del	XP_011542127.1:n.*465_*466del
XM_011543826.1:c.*465_*466del	XP_011542128.1:n.*465_*466del
XM_011543827.1:c.*465_*466del	XP_011542129.1:n.*465_*466del
NM_001330465.1:c.*465_*466del	NP_001317394.1:n.*465_*466del
XM_011543825.3:c.*465_*466del	XP_011542127.1:n.*465_*466del
NM_001715.3:c.*465_*466del MANE Select	NP_001706.2:n.*465_*466del
NM_001330465.2:c.*465_*466del	NP_001317394.1:n.*465_*466del