Canonical Allele Identifier: CA2448284754

Gene: BTK

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101359214_101359215delinsTA , CM000685.2:g.101359214_101359215delinsTA	GRCh38
NC_000023.10:g.100614202_100614203delinsTA , CM000685.1:g.100614202_100614203delinsTA	GRCh37
NC_000023.9:g.100500858_100500859delinsTA	NCBI36
NG_009616.1:g.32010_32011delinsTA , LRG_128:g.32010_32011delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000464006.2:n.674+78_674+79delinsTA
ENST00000478995.2:n.1054+78_1054+79delinsTA
ENST00000488970.2:n.1052+78_1052+79delinsTA
ENST00000695614.1:c.894+78_894+79delinsTA	ENSP00000512053.1:n.894+78_894+79delinsTA
ENST00000695615.1:c.894+78_894+79delinsTA	ENSP00000512054.1:n.894+78_894+79delinsTA
ENST00000695616.1:c.*739+78_*739+79delinsTA	ENSP00000512055.1:n.*739+78_*739+79delinsTA
ENST00000695617.1:c.891+78_891+79delinsTA	ENSP00000512056.1:n.891+78_891+79delinsTA
ENST00000695618.1:c.*643+78_*643+79delinsTA	ENSP00000512058.1:n.*643+78_*643+79delinsTA
ENST00000695619.1:c.*685-778_*685-777delinsTA	ENSP00000512059.1:n.*685-778_*685-777delinsTA
ENST00000695620.1:c.*739+78_*739+79delinsTA	ENSP00000512060.1:n.*739+78_*739+79delinsTA
ENST00000695621.1:c.894+78_894+79delinsTA	ENSP00000512061.1:n.894+78_894+79delinsTA
ENST00000695622.1:c.831+78_831+79delinsTA	ENSP00000512062.1:n.831+78_831+79delinsTA
ENST00000695623.1:c.888+78_888+79delinsTA	ENSP00000512063.1:n.888+78_888+79delinsTA
ENST00000695624.1:n.199+78_199+79delinsTA
ENST00000695625.1:c.894+78_894+79delinsTA	ENSP00000512064.1:n.894+78_894+79delinsTA
ENST00000703407.1:c.894+78_894+79delinsTA	ENSP00000512057.1:n.894+78_894+79delinsTA
ENST00000308731.8:c.894+78_894+79delinsTA MANE Select	ENSP00000308176.8:n.894+78_894+79delinsTA
ENST00000308731.7:c.894+78_894+79delinsTA	ENSP00000308176.7:n.894+78_894+79delinsTA
ENST00000372880.5:c.894+78_894+79delinsTA	ENSP00000361971.1:n.894+78_894+79delinsTA
ENST00000618050.4:c.894+78_894+79delinsTA	ENSP00000479125.1:n.894+78_894+79delinsTA
ENST00000621635.4:c.996+78_996+79delinsTA	ENSP00000483570.1:n.996+78_996+79delinsTA
NM_000061.2:c.894+78_894+79delinsTA , LRG_128t1:c.894+78_894+79delinsTA	NP_000052.1:n.894+78_894+79delinsTA
NM_001287344.1:c.996+78_996+79delinsTA	NP_001274273.1:n.996+78_996+79delinsTA
NM_001287345.1:c.894+78_894+79delinsTA	NP_001274274.1:n.894+78_894+79delinsTA
NM_000061.3:c.894+78_894+79delinsTA MANE Select	NP_000052.1:n.894+78_894+79delinsTA
NM_001287344.2:c.996+78_996+79delinsTA	NP_001274273.1:n.996+78_996+79delinsTA
NM_001287345.2:c.894+78_894+79delinsTA	NP_001274274.1:n.894+78_894+79delinsTA