Canonical Allele Identifier: CA413918407
Gene: BTK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101353205A>T , CM000685.2:g.101353205A>T GRCh38
NC_000023.10:g.100608193A>T , CM000685.1:g.100608193A>T GRCh37
NC_000023.9:g.100494849A>T NCBI36
NG_009616.1:g.38020T>A , LRG_128:g.38020T>A
NG_011734.1:g.765T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000478995.2:n.3414T>A
ENST00000488970.2:n.4053T>A
ENST00000695614.1:c.1897T>A ENSP00000512053.1:p.Cys633Ser
ENST00000695615.1:c.1897T>A ENSP00000512054.1:p.Cys633Ser
ENST00000695616.1:c.*1742T>A ENSP00000512055.1:n.*1742T>A
ENST00000695617.1:c.1894T>A ENSP00000512056.1:p.Cys632Ser
ENST00000695618.1:c.*1646T>A ENSP00000512058.1:n.*1646T>A
ENST00000695619.1:c.*1607T>A ENSP00000512059.1:n.*1607T>A
ENST00000695620.1:c.*1823T>A ENSP00000512060.1:n.*1823T>A
ENST00000695621.1:c.*322T>A ENSP00000512061.1:n.*322T>A
ENST00000695622.1:c.1834T>A ENSP00000512062.1:p.Cys612Ser
ENST00000695623.1:c.1891T>A ENSP00000512063.1:p.Cys631Ser
ENST00000695624.1:n.1202T>A
ENST00000695625.1:c.1875+22T>A ENSP00000512064.1:n.1875+22T>A
ENST00000695626.1:c.652T>A ENSP00000512065.1:n.652T>A
ENST00000695627.1:c.845T>A ENSP00000512066.1:n.845T>A
ENST00000695628.1:c.456T>A ENSP00000512067.1:n.456T>A
ENST00000695629.1:c.337T>A ENSP00000512068.1:p.Cys113Ser
ENST00000695630.1:c.624T>A
ENST00000695631.1:c.158T>A
ENST00000703407.1:c.1369T>A ENSP00000512057.1:p.Cys457Ser
ENST00000308731.8:c.1897T>A MANE Select ENSP00000308176.8:p.Cys633Ser
ENST00000308731.7:c.1897T>A ENSP00000308176.7:p.Cys633Ser
ENST00000372880.5:c.1369T>A ENSP00000361971.1:p.Cys457Ser
ENST00000470069.1:n.262T>A
ENST00000618050.4:c.1896T>A ENSP00000479125.1:n.1896T>A
ENST00000621635.4:c.1999T>A ENSP00000483570.1:p.Cys667Ser
NM_000061.2:c.1897T>A , LRG_128t1:c.1897T>A NP_000052.1:p.Cys633Ser
NM_001287344.1:c.1999T>A NP_001274273.1:p.Cys667Ser
NM_001287345.1:c.1369T>A NP_001274274.1:p.Cys457Ser
NM_000061.3:c.1897T>A MANE Select NP_000052.1:p.Cys633Ser
NM_001287344.2:c.1999T>A NP_001274273.1:p.Cys667Ser
NM_001287345.2:c.1369T>A NP_001274274.1:p.Cys457Ser