Canonical Allele Identifier: CA2694295009

Gene: BTK

Linked Data

• gnomAD v4: X-101353070-T-TAAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101353081_101353085dup , CM000685.2:g.101353081_101353085dup	GRCh38
NC_000023.10:g.100608069_100608073dup , CM000685.1:g.100608069_100608073dup	GRCh37
NC_000023.9:g.100494725_100494729dup	NCBI36
NG_009616.1:g.38150_38154dup , LRG_128:g.38150_38154dup
NG_011734.1:g.895_899dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478995.2:n.3425+119_3425+123dup
ENST00000488970.2:n.4064+119_4064+123dup
ENST00000695614.1:c.1908+119_1908+123dup	ENSP00000512053.1:n.1908+119_1908+123dup
ENST00000695615.1:c.1908+119_1908+123dup	ENSP00000512054.1:n.1908+119_1908+123dup
ENST00000695616.1:c.*1753+119_*1753+123dup	ENSP00000512055.1:n.*1753+119_*1753+123dup
ENST00000695617.1:c.1905+119_1905+123dup	ENSP00000512056.1:n.1905+119_1905+123dup
ENST00000695618.1:c.*1657+119_*1657+123dup	ENSP00000512058.1:n.*1657+119_*1657+123dup
ENST00000695619.1:c.*1618+119_*1618+123dup	ENSP00000512059.1:n.*1618+119_*1618+123dup
ENST00000695620.1:c.*1834+119_*1834+123dup	ENSP00000512060.1:n.*1834+119_*1834+123dup
ENST00000695621.1:c.*333+119_*333+123dup	ENSP00000512061.1:n.*333+119_*333+123dup
ENST00000695622.1:c.1845+119_1845+123dup	ENSP00000512062.1:n.1845+119_1845+123dup
ENST00000695623.1:c.1902+119_1902+123dup	ENSP00000512063.1:n.1902+119_1902+123dup
ENST00000695624.1:n.1213+119_1213+123dup
ENST00000695625.1:c.1875+152_1875+156dup	ENSP00000512064.1:n.1875+152_1875+156dup
ENST00000695626.1:c.663+119_663+123dup	ENSP00000512065.1:n.663+119_663+123dup
ENST00000695627.1:c.856+119_856+123dup	ENSP00000512066.1:n.856+119_856+123dup
ENST00000695628.1:c.467+119_467+123dup	ENSP00000512067.1:n.467+119_467+123dup
ENST00000695629.1:c.348+119_348+123dup	ENSP00000512068.1:n.348+119_348+123dup
ENST00000695630.1:c.635+119_635+123dup
ENST00000695631.1:c.169+119_169+123dup
ENST00000703407.1:c.1380+119_1380+123dup	ENSP00000512057.1:n.1380+119_1380+123dup
ENST00000308731.8:c.1908+119_1908+123dup MANE Select	ENSP00000308176.8:n.1908+119_1908+123dup
ENST00000308731.7:c.1908+119_1908+123dup	ENSP00000308176.7:n.1908+119_1908+123dup
ENST00000372880.5:c.1380+119_1380+123dup	ENSP00000361971.1:n.1380+119_1380+123dup
ENST00000470069.1:n.392_396dup
ENST00000618050.4:c.1907+119_1907+123dup	ENSP00000479125.1:n.1907+119_1907+123dup
ENST00000621635.4:c.2010+119_2010+123dup	ENSP00000483570.1:n.2010+119_2010+123dup
NM_000061.2:c.1908+119_1908+123dup , LRG_128t1:c.1908+119_1908+123dup	NP_000052.1:n.1908+119_1908+123dup
NM_001287344.1:c.2010+119_2010+123dup	NP_001274273.1:n.2010+119_2010+123dup
NM_001287345.1:c.1380+119_1380+123dup	NP_001274274.1:n.1380+119_1380+123dup
NM_000061.3:c.1908+119_1908+123dup MANE Select	NP_000052.1:n.1908+119_1908+123dup
NM_001287344.2:c.2010+119_2010+123dup	NP_001274273.1:n.2010+119_2010+123dup
NM_001287345.2:c.1380+119_1380+123dup	NP_001274274.1:n.1380+119_1380+123dup