Canonical Allele Identifier: CA517531103

Gene: BTK

Linked Data

• MyVariant Identifiers: chrX:g.100608937G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101353949G>T , CM000685.2:g.101353949G>T	GRCh38
NC_000023.10:g.100608937G>T , CM000685.1:g.100608937G>T	GRCh37
NC_000023.9:g.100495593G>T	NCBI36
NG_009616.1:g.37276C>A , LRG_128:g.37276C>A
NG_011734.1:g.21C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478995.2:n.3188C>A
ENST00000488970.2:n.3827C>A
ENST00000695614.1:c.1671C>A	ENSP00000512053.1:p.Ser557=
ENST00000695615.1:c.1671C>A	ENSP00000512054.1:p.Ser557=
ENST00000695616.1:c.*1516C>A	ENSP00000512055.1:n.*1516C>A
ENST00000695617.1:c.1668C>A	ENSP00000512056.1:p.Ser556=
ENST00000695618.1:c.*1420C>A	ENSP00000512058.1:n.*1420C>A
ENST00000695619.1:c.*1381C>A	ENSP00000512059.1:n.*1381C>A
ENST00000695620.1:c.*1597C>A	ENSP00000512060.1:n.*1597C>A
ENST00000695621.1:c.*96C>A	ENSP00000512061.1:n.*96C>A
ENST00000695622.1:c.1608C>A	ENSP00000512062.1:p.Ser536=
ENST00000695623.1:c.1665C>A	ENSP00000512063.1:p.Ser555=
ENST00000695624.1:n.976C>A
ENST00000695625.1:c.1671C>A	ENSP00000512064.1:p.Ser557=
ENST00000695626.1:c.426C>A	ENSP00000512065.1:n.426C>A
ENST00000695627.1:c.619C>A	ENSP00000512066.1:n.619C>A
ENST00000695628.1:c.230C>A	ENSP00000512067.1:n.230C>A
ENST00000695629.1:c.191-598C>A	ENSP00000512068.1:n.191-598C>A
ENST00000695630.1:c.398C>A
ENST00000695631.1:c.115-701C>A
ENST00000695632.1:n.471C>A
ENST00000703407.1:c.1143C>A	ENSP00000512057.1:p.Ser381=
ENST00000308731.8:c.1671C>A MANE Select	ENSP00000308176.8:p.Ser557=
ENST00000308731.7:c.1671C>A	ENSP00000308176.7:p.Ser557=
ENST00000372880.5:c.1143C>A	ENSP00000361971.1:p.Ser381=
ENST00000470069.1:n.36C>A
ENST00000488970.1:n.273C>A
ENST00000618050.4:c.1671C>A	ENSP00000479125.1:p.Ser557=
ENST00000621635.4:c.1773C>A	ENSP00000483570.1:p.Ser591=
NM_000061.2:c.1671C>A , LRG_128t1:c.1671C>A	NP_000052.1:p.Ser557=
NM_001287344.1:c.1773C>A	NP_001274273.1:p.Ser591=
NM_001287345.1:c.1143C>A	NP_001274274.1:p.Ser381=
NM_000061.3:c.1671C>A MANE Select	NP_000052.1:p.Ser557=
NM_001287344.2:c.1773C>A	NP_001274273.1:p.Ser591=
NM_001287345.2:c.1143C>A	NP_001274274.1:p.Ser381=