Canonical Allele Identifier: CA2448283037

Gene: BTK

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101353279T= , CM000685.2:g.101353279T=	GRCh38
NC_000023.10:g.100608267T= , CM000685.1:g.100608267T=	GRCh37
NC_000023.9:g.100494923T=	NCBI36
NG_009616.1:g.37946A= , LRG_128:g.37946A=
NG_011734.1:g.691A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478995.2:n.3340A=
ENST00000488970.2:n.3979A=
ENST00000695614.1:c.1823A=	ENSP00000512053.1:p.Glu608=
ENST00000695615.1:c.1823A=	ENSP00000512054.1:p.Glu608=
ENST00000695616.1:c.*1668A=	ENSP00000512055.1:n.*1668A=
ENST00000695617.1:c.1820A=	ENSP00000512056.1:p.Glu607=
ENST00000695618.1:c.*1572A=	ENSP00000512058.1:n.*1572A=
ENST00000695619.1:c.*1533A=	ENSP00000512059.1:n.*1533A=
ENST00000695620.1:c.*1749A=	ENSP00000512060.1:n.*1749A=
ENST00000695621.1:c.*248A=	ENSP00000512061.1:n.*248A=
ENST00000695622.1:c.1760A=	ENSP00000512062.1:p.Glu587=
ENST00000695623.1:c.1817A=	ENSP00000512063.1:p.Glu606=
ENST00000695624.1:n.1128A=
ENST00000695625.1:c.1823A=	ENSP00000512064.1:p.Glu608=
ENST00000695626.1:c.578A=	ENSP00000512065.1:n.578A=
ENST00000695627.1:c.771A=	ENSP00000512066.1:n.771A=
ENST00000695628.1:c.382A=	ENSP00000512067.1:n.382A=
ENST00000695629.1:c.263A=	ENSP00000512068.1:p.Glu88=
ENST00000695630.1:c.550A=
ENST00000695631.1:c.115-31A=
ENST00000703407.1:c.1295A=	ENSP00000512057.1:p.Glu432=
ENST00000308731.8:c.1823A= MANE Select	ENSP00000308176.8:p.Glu608=
ENST00000308731.7:c.1823A=	ENSP00000308176.7:p.Glu608=
ENST00000372880.5:c.1295A=	ENSP00000361971.1:p.Glu432=
ENST00000470069.1:n.188A=
ENST00000618050.4:c.1822A=	ENSP00000479125.1:n.1822A=
ENST00000621635.4:c.1925A=	ENSP00000483570.1:p.Glu642=
NM_000061.2:c.1823A= , LRG_128t1:c.1823A=	NP_000052.1:p.Glu608=
NM_001287344.1:c.1925A=	NP_001274273.1:p.Glu642=
NM_001287345.1:c.1295A=	NP_001274274.1:p.Glu432=
NM_000061.3:c.1823A= MANE Select	NP_000052.1:p.Glu608=
NM_001287344.2:c.1925A=	NP_001274273.1:p.Glu642=
NM_001287345.2:c.1295A=	NP_001274274.1:p.Glu432=