Canonical Allele Identifier: CA413918825
Gene: BTK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101353251G>T , CM000685.2:g.101353251G>T GRCh38
NC_000023.10:g.100608239G>T , CM000685.1:g.100608239G>T GRCh37
NC_000023.9:g.100494895G>T NCBI36
NG_009616.1:g.37974C>A , LRG_128:g.37974C>A
NG_011734.1:g.719C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000478995.2:n.3368C>A
ENST00000488970.2:n.4007C>A
ENST00000695614.1:c.1851C>A ENSP00000512053.1:p.Tyr617Ter
ENST00000695615.1:c.1851C>A ENSP00000512054.1:p.Tyr617Ter
ENST00000695616.1:c.*1696C>A ENSP00000512055.1:n.*1696C>A
ENST00000695617.1:c.1848C>A ENSP00000512056.1:p.Tyr616Ter
ENST00000695618.1:c.*1600C>A ENSP00000512058.1:n.*1600C>A
ENST00000695619.1:c.*1561C>A ENSP00000512059.1:n.*1561C>A
ENST00000695620.1:c.*1777C>A ENSP00000512060.1:n.*1777C>A
ENST00000695621.1:c.*276C>A ENSP00000512061.1:n.*276C>A
ENST00000695622.1:c.1788C>A ENSP00000512062.1:p.Tyr596Ter
ENST00000695623.1:c.1845C>A ENSP00000512063.1:p.Tyr615Ter
ENST00000695624.1:n.1156C>A
ENST00000695625.1:c.1851C>A ENSP00000512064.1:p.Tyr617Ter
ENST00000695626.1:c.606C>A ENSP00000512065.1:n.606C>A
ENST00000695627.1:c.799C>A ENSP00000512066.1:n.799C>A
ENST00000695628.1:c.410C>A ENSP00000512067.1:n.410C>A
ENST00000695629.1:c.291C>A ENSP00000512068.1:p.Tyr97Ter
ENST00000695630.1:c.578C>A
ENST00000695631.1:c.115-3C>A
ENST00000703407.1:c.1323C>A ENSP00000512057.1:p.Tyr441Ter
ENST00000308731.8:c.1851C>A MANE Select ENSP00000308176.8:p.Tyr617Ter
ENST00000308731.7:c.1851C>A ENSP00000308176.7:p.Tyr617Ter
ENST00000372880.5:c.1323C>A ENSP00000361971.1:p.Tyr441Ter
ENST00000470069.1:n.216C>A
ENST00000618050.4:c.1850C>A ENSP00000479125.1:n.1850C>A
ENST00000621635.4:c.1953C>A ENSP00000483570.1:p.Tyr651Ter
NM_000061.2:c.1851C>A , LRG_128t1:c.1851C>A NP_000052.1:p.Tyr617Ter
NM_001287344.1:c.1953C>A NP_001274273.1:p.Tyr651Ter
NM_001287345.1:c.1323C>A NP_001274274.1:p.Tyr441Ter
NM_000061.3:c.1851C>A MANE Select NP_000052.1:p.Tyr617Ter
NM_001287344.2:c.1953C>A NP_001274273.1:p.Tyr651Ter
NM_001287345.2:c.1323C>A NP_001274274.1:p.Tyr441Ter