Canonical Allele Identifier: CA2694294944

Gene: BTK

Linked Data

• gnomAD v4: X-101353054-AGACCTT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101353056_101353061del , CM000685.2:g.101353056_101353061del	GRCh38
NC_000023.10:g.100608044_100608049del , CM000685.1:g.100608044_100608049del	GRCh37
NC_000023.9:g.100494700_100494705del	NCBI36
NG_009616.1:g.38165_38170del , LRG_128:g.38165_38170del
NG_011734.1:g.910_915del

Transcript Alleles

HGVS	Amino-acid change
ENST00000478995.2:n.3425+134_3425+139del
ENST00000488970.2:n.4064+134_4064+139del
ENST00000695614.1:c.1908+134_1908+139del	ENSP00000512053.1:n.1908+134_1908+139del
ENST00000695615.1:c.1908+134_1908+139del	ENSP00000512054.1:n.1908+134_1908+139del
ENST00000695616.1:c.*1753+134_*1753+139del	ENSP00000512055.1:n.*1753+134_*1753+139del
ENST00000695617.1:c.1905+134_1905+139del	ENSP00000512056.1:n.1905+134_1905+139del
ENST00000695618.1:c.*1657+134_*1657+139del	ENSP00000512058.1:n.*1657+134_*1657+139del
ENST00000695619.1:c.*1618+134_*1618+139del	ENSP00000512059.1:n.*1618+134_*1618+139del
ENST00000695620.1:c.*1834+134_*1834+139del	ENSP00000512060.1:n.*1834+134_*1834+139del
ENST00000695621.1:c.*333+134_*333+139del	ENSP00000512061.1:n.*333+134_*333+139del
ENST00000695622.1:c.1845+134_1845+139del	ENSP00000512062.1:n.1845+134_1845+139del
ENST00000695623.1:c.1902+134_1902+139del	ENSP00000512063.1:n.1902+134_1902+139del
ENST00000695624.1:n.1213+134_1213+139del
ENST00000695625.1:c.1875+167_1875+172del	ENSP00000512064.1:n.1875+167_1875+172del
ENST00000695626.1:c.663+134_663+139del	ENSP00000512065.1:n.663+134_663+139del
ENST00000695627.1:c.856+134_856+139del	ENSP00000512066.1:n.856+134_856+139del
ENST00000695628.1:c.467+134_467+139del	ENSP00000512067.1:n.467+134_467+139del
ENST00000695629.1:c.348+134_348+139del	ENSP00000512068.1:n.348+134_348+139del
ENST00000695630.1:c.635+134_635+139del
ENST00000695631.1:c.169+134_169+139del
ENST00000703407.1:c.1380+134_1380+139del	ENSP00000512057.1:n.1380+134_1380+139del
ENST00000308731.8:c.1908+134_1908+139del MANE Select	ENSP00000308176.8:n.1908+134_1908+139del
ENST00000308731.7:c.1908+134_1908+139del	ENSP00000308176.7:n.1908+134_1908+139del
ENST00000372880.5:c.1380+134_1380+139del	ENSP00000361971.1:n.1380+134_1380+139del
ENST00000470069.1:n.407_412del
ENST00000618050.4:c.1907+134_1907+139del	ENSP00000479125.1:n.1907+134_1907+139del
ENST00000621635.4:c.2010+134_2010+139del	ENSP00000483570.1:n.2010+134_2010+139del
NM_000061.2:c.1908+134_1908+139del , LRG_128t1:c.1908+134_1908+139del	NP_000052.1:n.1908+134_1908+139del
NM_001287344.1:c.2010+134_2010+139del	NP_001274273.1:n.2010+134_2010+139del
NM_001287345.1:c.1380+134_1380+139del	NP_001274274.1:n.1380+134_1380+139del
NM_000061.3:c.1908+134_1908+139del MANE Select	NP_000052.1:n.1908+134_1908+139del
NM_001287344.2:c.2010+134_2010+139del	NP_001274273.1:n.2010+134_2010+139del
NM_001287345.2:c.1380+134_1380+139del	NP_001274274.1:n.1380+134_1380+139del