Canonical Allele Identifier: CA2448283045
Gene: BTK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101353311T= , CM000685.2:g.101353311T= GRCh38
NC_000023.10:g.100608299T= , CM000685.1:g.100608299T= GRCh37
NC_000023.9:g.100494955T= NCBI36
NG_009616.1:g.37914A= , LRG_128:g.37914A=
NG_011734.1:g.659A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000478995.2:n.3308A=
ENST00000488970.2:n.3947A=
ENST00000695614.1:c.1791A= ENSP00000512053.1:p.Pro597=
ENST00000695615.1:c.1791A= ENSP00000512054.1:p.Pro597=
ENST00000695616.1:c.*1636A= ENSP00000512055.1:n.*1636A=
ENST00000695617.1:c.1788A= ENSP00000512056.1:p.Pro596=
ENST00000695618.1:c.*1540A= ENSP00000512058.1:n.*1540A=
ENST00000695619.1:c.*1501A= ENSP00000512059.1:n.*1501A=
ENST00000695620.1:c.*1717A= ENSP00000512060.1:n.*1717A=
ENST00000695621.1:c.*216A= ENSP00000512061.1:n.*216A=
ENST00000695622.1:c.1728A= ENSP00000512062.1:p.Pro576=
ENST00000695623.1:c.1785A= ENSP00000512063.1:p.Pro595=
ENST00000695624.1:n.1096A=
ENST00000695625.1:c.1791A= ENSP00000512064.1:p.Pro597=
ENST00000695626.1:c.546A= ENSP00000512065.1:n.546A=
ENST00000695627.1:c.739A= ENSP00000512066.1:n.739A=
ENST00000695628.1:c.350A= ENSP00000512067.1:n.350A=
ENST00000695629.1:c.231A= ENSP00000512068.1:p.Pro77=
ENST00000695630.1:c.518A=
ENST00000695631.1:c.115-63A=
ENST00000703407.1:c.1263A= ENSP00000512057.1:p.Pro421=
ENST00000308731.8:c.1791A= MANE Select ENSP00000308176.8:p.Pro597=
ENST00000308731.7:c.1791A= ENSP00000308176.7:p.Pro597=
ENST00000372880.5:c.1263A= ENSP00000361971.1:p.Pro421=
ENST00000470069.1:n.156A=
ENST00000618050.4:c.1790A= ENSP00000479125.1:n.1790A=
ENST00000621635.4:c.1893A= ENSP00000483570.1:p.Pro631=
NM_000061.2:c.1791A= , LRG_128t1:c.1791A= NP_000052.1:p.Pro597=
NM_001287344.1:c.1893A= NP_001274273.1:p.Pro631=
NM_001287345.1:c.1263A= NP_001274274.1:p.Pro421=
NM_000061.3:c.1791A= MANE Select NP_000052.1:p.Pro597=
NM_001287344.2:c.1893A= NP_001274273.1:p.Pro631=
NM_001287345.2:c.1263A= NP_001274274.1:p.Pro421=