Canonical Allele Identifier: CA2448281903
Gene: BTK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101349827A= , CM000685.2:g.101349827A= GRCh38
NC_000023.10:g.100604815A= , CM000685.1:g.100604815A= GRCh37
NC_000023.9:g.100491471A= NCBI36
NG_009616.1:g.41398T= , LRG_128:g.41398T=
NG_011734.1:g.4143T=

Transcript Alleles

HGVS Amino-acid change
ENST00000478995.2:n.3555T=
ENST00000488970.2:n.4194T=
ENST00000695614.1:c.*58T= ENSP00000512053.1:n.*58T=
ENST00000695615.1:c.*58T= ENSP00000512054.1:n.*58T=
ENST00000695616.1:c.*1883T= ENSP00000512055.1:n.*1883T=
ENST00000695617.1:c.*58T= ENSP00000512056.1:n.*58T=
ENST00000695618.1:c.*1787T= ENSP00000512058.1:n.*1787T=
ENST00000695619.1:c.*1748T= ENSP00000512059.1:n.*1748T=
ENST00000695620.1:c.*1964T= ENSP00000512060.1:n.*1964T=
ENST00000695621.1:c.*463T= ENSP00000512061.1:n.*463T=
ENST00000695622.1:c.*58T= ENSP00000512062.1:n.*58T=
ENST00000695623.1:c.*58T= ENSP00000512063.1:n.*58T=
ENST00000695624.1:n.1343T=
ENST00000695625.1:c.*58T= ENSP00000512064.1:n.*58T=
ENST00000695626.1:c.793T= ENSP00000512065.1:n.793T=
ENST00000695627.1:c.986T= ENSP00000512066.1:n.986T=
ENST00000695628.1:c.597T= ENSP00000512067.1:n.597T=
ENST00000695629.1:c.478T= ENSP00000512068.1:n.478T=
ENST00000703407.1:c.*58T= ENSP00000512057.1:n.*58T=
ENST00000308731.8:c.*58T= MANE Select ENSP00000308176.8:n.*58T=
ENST00000308731.7:c.*58T= ENSP00000308176.7:n.*58T=
ENST00000372880.5:c.*58T= ENSP00000361971.1:n.*58T=
ENST00000618050.4:c.2037T= ENSP00000479125.1:n.2037T=
ENST00000621635.4:c.*58T= ENSP00000483570.1:n.*58T=
NM_000061.2:c.*58T= , LRG_128t1:c.*58T= NP_000052.1:n.*58T=
NM_001287344.1:c.*58T= NP_001274273.1:n.*58T=
NM_001287345.1:c.*58T= NP_001274274.1:n.*58T=
NM_000061.3:c.*58T= MANE Select NP_000052.1:n.*58T=
NM_001287344.2:c.*58T= NP_001274273.1:n.*58T=
NM_001287345.2:c.*58T= NP_001274274.1:n.*58T=