Canonical Allele Identifier: CA1763964007

Gene: BLK

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11564285_11564286delinsAC , CM000670.2:g.11564285_11564286delinsAC	GRCh38
NC_000008.10:g.11421794_11421795delinsAC , CM000670.1:g.11421794_11421795delinsAC	GRCh37
NC_000008.9:g.11459203_11459204delinsAC	NCBI36
NG_023543.1:g.75274_75275delinsAC
NG_023543.2:g.75274_75275delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.1803_1804delinsAC
ENST00000696154.1:c.*1013_*1014delinsAC	ENSP00000512445.1:n.*1013_*1014delinsAC
ENST00000696155.1:n.579_580delinsAC
ENST00000259089.9:c.*177_*178delinsAC MANE Select	ENSP00000259089.4:n.*177_*178delinsAC
ENST00000645242.1:c.*177_*178delinsAC	ENSP00000494690.1:n.*177_*178delinsAC
ENST00000259089.8:c.*177_*178delinsAC	ENSP00000259089.4:n.*177_*178delinsAC
ENST00000526097.1:n.1635_1636delinsAC
ENST00000529894.1:c.*177_*178delinsAC	ENSP00000433663.1:n.*177_*178delinsAC
NM_001715.2:c.*177_*178delinsAC	NP_001706.2:n.*177_*178delinsAC
XM_011543824.1:c.*177_*178delinsAC	XP_011542126.1:n.*177_*178delinsAC
XM_011543825.1:c.*177_*178delinsAC	XP_011542127.1:n.*177_*178delinsAC
XM_011543826.1:c.*177_*178delinsAC	XP_011542128.1:n.*177_*178delinsAC
XM_011543827.1:c.*177_*178delinsAC	XP_011542129.1:n.*177_*178delinsAC
NM_001330465.1:c.*177_*178delinsAC	NP_001317394.1:n.*177_*178delinsAC
XM_011543825.3:c.*177_*178delinsAC	XP_011542127.1:n.*177_*178delinsAC
NM_001715.3:c.*177_*178delinsAC MANE Select	NP_001706.2:n.*177_*178delinsAC
NM_001330465.2:c.*177_*178delinsAC	NP_001317394.1:n.*177_*178delinsAC