Canonical Allele Identifier: CA413919068
Gene: BTK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101353282G>C , CM000685.2:g.101353282G>C GRCh38
NC_000023.10:g.100608270G>C , CM000685.1:g.100608270G>C GRCh37
NC_000023.9:g.100494926G>C NCBI36
NG_009616.1:g.37943C>G , LRG_128:g.37943C>G
NG_011734.1:g.688C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000478995.2:n.3337C>G
ENST00000488970.2:n.3976C>G
ENST00000695614.1:c.1820C>G ENSP00000512053.1:p.Ala607Gly
ENST00000695615.1:c.1820C>G ENSP00000512054.1:p.Ala607Gly
ENST00000695616.1:c.*1665C>G ENSP00000512055.1:n.*1665C>G
ENST00000695617.1:c.1817C>G ENSP00000512056.1:p.Ala606Gly
ENST00000695618.1:c.*1569C>G ENSP00000512058.1:n.*1569C>G
ENST00000695619.1:c.*1530C>G ENSP00000512059.1:n.*1530C>G
ENST00000695620.1:c.*1746C>G ENSP00000512060.1:n.*1746C>G
ENST00000695621.1:c.*245C>G ENSP00000512061.1:n.*245C>G
ENST00000695622.1:c.1757C>G ENSP00000512062.1:p.Ala586Gly
ENST00000695623.1:c.1814C>G ENSP00000512063.1:p.Ala605Gly
ENST00000695624.1:n.1125C>G
ENST00000695625.1:c.1820C>G ENSP00000512064.1:p.Ala607Gly
ENST00000695626.1:c.575C>G ENSP00000512065.1:n.575C>G
ENST00000695627.1:c.768C>G ENSP00000512066.1:n.768C>G
ENST00000695628.1:c.379C>G ENSP00000512067.1:n.379C>G
ENST00000695629.1:c.260C>G ENSP00000512068.1:p.Ala87Gly
ENST00000695630.1:c.547C>G
ENST00000695631.1:c.115-34C>G
ENST00000703407.1:c.1292C>G ENSP00000512057.1:p.Ala431Gly
ENST00000308731.8:c.1820C>G MANE Select ENSP00000308176.8:p.Ala607Gly
ENST00000308731.7:c.1820C>G ENSP00000308176.7:p.Ala607Gly
ENST00000372880.5:c.1292C>G ENSP00000361971.1:p.Ala431Gly
ENST00000470069.1:n.185C>G
ENST00000618050.4:c.1819C>G ENSP00000479125.1:n.1819C>G
ENST00000621635.4:c.1922C>G ENSP00000483570.1:p.Ala641Gly
NM_000061.2:c.1820C>G , LRG_128t1:c.1820C>G NP_000052.1:p.Ala607Gly
NM_001287344.1:c.1922C>G NP_001274273.1:p.Ala641Gly
NM_001287345.1:c.1292C>G NP_001274274.1:p.Ala431Gly
NM_000061.3:c.1820C>G MANE Select NP_000052.1:p.Ala607Gly
NM_001287344.2:c.1922C>G NP_001274273.1:p.Ala641Gly
NM_001287345.2:c.1292C>G NP_001274274.1:p.Ala431Gly