Canonical Allele Identifier: CA413918360
Gene: BTK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101353201C>A , CM000685.2:g.101353201C>A GRCh38
NC_000023.10:g.100608189C>A , CM000685.1:g.100608189C>A GRCh37
NC_000023.9:g.100494845C>A NCBI36
NG_009616.1:g.38024G>T , LRG_128:g.38024G>T
NG_011734.1:g.769G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000478995.2:n.3418G>T
ENST00000488970.2:n.4057G>T
ENST00000695614.1:c.1901G>T ENSP00000512053.1:p.Trp634Leu
ENST00000695615.1:c.1901G>T ENSP00000512054.1:p.Trp634Leu
ENST00000695616.1:c.*1746G>T ENSP00000512055.1:n.*1746G>T
ENST00000695617.1:c.1898G>T ENSP00000512056.1:p.Trp633Leu
ENST00000695618.1:c.*1650G>T ENSP00000512058.1:n.*1650G>T
ENST00000695619.1:c.*1611G>T ENSP00000512059.1:n.*1611G>T
ENST00000695620.1:c.*1827G>T ENSP00000512060.1:n.*1827G>T
ENST00000695621.1:c.*326G>T ENSP00000512061.1:n.*326G>T
ENST00000695622.1:c.1838G>T ENSP00000512062.1:p.Trp613Leu
ENST00000695623.1:c.1895G>T ENSP00000512063.1:p.Trp632Leu
ENST00000695624.1:n.1206G>T
ENST00000695625.1:c.1875+26G>T ENSP00000512064.1:n.1875+26G>T
ENST00000695626.1:c.656G>T ENSP00000512065.1:n.656G>T
ENST00000695627.1:c.849G>T ENSP00000512066.1:n.849G>T
ENST00000695628.1:c.460G>T ENSP00000512067.1:n.460G>T
ENST00000695629.1:c.341G>T ENSP00000512068.1:p.Trp114Leu
ENST00000695630.1:c.628G>T
ENST00000695631.1:c.162G>T
ENST00000703407.1:c.1373G>T ENSP00000512057.1:p.Trp458Leu
ENST00000308731.8:c.1901G>T MANE Select ENSP00000308176.8:p.Trp634Leu
ENST00000308731.7:c.1901G>T ENSP00000308176.7:p.Trp634Leu
ENST00000372880.5:c.1373G>T ENSP00000361971.1:p.Trp458Leu
ENST00000470069.1:n.266G>T
ENST00000618050.4:c.1900G>T ENSP00000479125.1:n.1900G>T
ENST00000621635.4:c.2003G>T ENSP00000483570.1:p.Trp668Leu
NM_000061.2:c.1901G>T , LRG_128t1:c.1901G>T NP_000052.1:p.Trp634Leu
NM_001287344.1:c.2003G>T NP_001274273.1:p.Trp668Leu
NM_001287345.1:c.1373G>T NP_001274274.1:p.Trp458Leu
NM_000061.3:c.1901G>T MANE Select NP_000052.1:p.Trp634Leu
NM_001287344.2:c.2003G>T NP_001274273.1:p.Trp668Leu
NM_001287345.2:c.1373G>T NP_001274274.1:p.Trp458Leu