Canonical Allele Identifier: CA517529599

Gene: BTK

Linked Data

• MyVariant Identifiers: chrX:g.100608236C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101353248C>T , CM000685.2:g.101353248C>T	GRCh38
NC_000023.10:g.100608236C>T , CM000685.1:g.100608236C>T	GRCh37
NC_000023.9:g.100494892C>T	NCBI36
NG_009616.1:g.37977G>A , LRG_128:g.37977G>A
NG_011734.1:g.722G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478995.2:n.3371G>A
ENST00000488970.2:n.4010G>A
ENST00000695614.1:c.1854G>A	ENSP00000512053.1:p.Arg618=
ENST00000695615.1:c.1854G>A	ENSP00000512054.1:p.Arg618=
ENST00000695616.1:c.*1699G>A	ENSP00000512055.1:n.*1699G>A
ENST00000695617.1:c.1851G>A	ENSP00000512056.1:p.Arg617=
ENST00000695618.1:c.*1603G>A	ENSP00000512058.1:n.*1603G>A
ENST00000695619.1:c.*1564G>A	ENSP00000512059.1:n.*1564G>A
ENST00000695620.1:c.*1780G>A	ENSP00000512060.1:n.*1780G>A
ENST00000695621.1:c.*279G>A	ENSP00000512061.1:n.*279G>A
ENST00000695622.1:c.1791G>A	ENSP00000512062.1:p.Arg597=
ENST00000695623.1:c.1848G>A	ENSP00000512063.1:p.Arg616=
ENST00000695624.1:n.1159G>A
ENST00000695625.1:c.1854G>A	ENSP00000512064.1:p.Arg618=
ENST00000695626.1:c.609G>A	ENSP00000512065.1:n.609G>A
ENST00000695627.1:c.802G>A	ENSP00000512066.1:n.802G>A
ENST00000695628.1:c.413G>A	ENSP00000512067.1:n.413G>A
ENST00000695629.1:c.294G>A	ENSP00000512068.1:p.Arg98=
ENST00000695630.1:c.581G>A
ENST00000695631.1:c.115G>A
ENST00000703407.1:c.1326G>A	ENSP00000512057.1:p.Arg442=
ENST00000308731.8:c.1854G>A MANE Select	ENSP00000308176.8:p.Arg618=
ENST00000308731.7:c.1854G>A	ENSP00000308176.7:p.Arg618=
ENST00000372880.5:c.1326G>A	ENSP00000361971.1:p.Arg442=
ENST00000470069.1:n.219G>A
ENST00000618050.4:c.1853G>A	ENSP00000479125.1:n.1853G>A
ENST00000621635.4:c.1956G>A	ENSP00000483570.1:p.Arg652=
NM_000061.2:c.1854G>A , LRG_128t1:c.1854G>A	NP_000052.1:p.Arg618=
NM_001287344.1:c.1956G>A	NP_001274273.1:p.Arg652=
NM_001287345.1:c.1326G>A	NP_001274274.1:p.Arg442=
NM_000061.3:c.1854G>A MANE Select	NP_000052.1:p.Arg618=
NM_001287344.2:c.1956G>A	NP_001274273.1:p.Arg652=
NM_001287345.2:c.1326G>A	NP_001274274.1:p.Arg442=