Canonical Allele Identifier: CA413919560

Gene: BTK

Linked Data

• MyVariant Identifiers: chrX:g.100608328A>T (hg19) ; chrX:g.101353340A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101353340A>T , CM000685.2:g.101353340A>T	GRCh38
NC_000023.10:g.100608328A>T , CM000685.1:g.100608328A>T	GRCh37
NC_000023.9:g.100494984A>T	NCBI36
NG_009616.1:g.37885T>A , LRG_128:g.37885T>A
NG_011734.1:g.630T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478995.2:n.3279T>A
ENST00000488970.2:n.3918T>A
ENST00000695614.1:c.1762T>A	ENSP00000512053.1:p.Trp588Arg
ENST00000695615.1:c.1762T>A	ENSP00000512054.1:p.Trp588Arg
ENST00000695616.1:c.*1607T>A	ENSP00000512055.1:n.*1607T>A
ENST00000695617.1:c.1759T>A	ENSP00000512056.1:p.Trp587Arg
ENST00000695618.1:c.*1511T>A	ENSP00000512058.1:n.*1511T>A
ENST00000695619.1:c.*1472T>A	ENSP00000512059.1:n.*1472T>A
ENST00000695620.1:c.*1688T>A	ENSP00000512060.1:n.*1688T>A
ENST00000695621.1:c.*187T>A	ENSP00000512061.1:n.*187T>A
ENST00000695622.1:c.1699T>A	ENSP00000512062.1:p.Trp567Arg
ENST00000695623.1:c.1756T>A	ENSP00000512063.1:p.Trp586Arg
ENST00000695624.1:n.1067T>A
ENST00000695625.1:c.1762T>A	ENSP00000512064.1:p.Trp588Arg
ENST00000695626.1:c.517T>A	ENSP00000512065.1:n.517T>A
ENST00000695627.1:c.710T>A	ENSP00000512066.1:n.710T>A
ENST00000695628.1:c.321T>A	ENSP00000512067.1:n.321T>A
ENST00000695629.1:c.202T>A	ENSP00000512068.1:p.Trp68Arg
ENST00000695630.1:c.489T>A
ENST00000695631.1:c.115-92T>A
ENST00000703407.1:c.1234T>A	ENSP00000512057.1:p.Trp412Arg
ENST00000308731.8:c.1762T>A MANE Select	ENSP00000308176.8:p.Trp588Arg
ENST00000308731.7:c.1762T>A	ENSP00000308176.7:p.Trp588Arg
ENST00000372880.5:c.1234T>A	ENSP00000361971.1:p.Trp412Arg
ENST00000470069.1:n.127T>A
ENST00000488970.1:n.364T>A
ENST00000618050.4:c.1761T>A	ENSP00000479125.1:n.1761T>A
ENST00000621635.4:c.1864T>A	ENSP00000483570.1:p.Trp622Arg
NM_000061.2:c.1762T>A , LRG_128t1:c.1762T>A	NP_000052.1:p.Trp588Arg
NM_001287344.1:c.1864T>A	NP_001274273.1:p.Trp622Arg
NM_001287345.1:c.1234T>A	NP_001274274.1:p.Trp412Arg
NM_000061.3:c.1762T>A MANE Select	NP_000052.1:p.Trp588Arg
NM_001287344.2:c.1864T>A	NP_001274273.1:p.Trp622Arg
NM_001287345.2:c.1234T>A	NP_001274274.1:p.Trp412Arg