Canonical Allele Identifier: CA2448283032

Gene: BTK

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101353259G= , CM000685.2:g.101353259G=	GRCh38
NC_000023.10:g.100608247G= , CM000685.1:g.100608247G=	GRCh37
NC_000023.9:g.100494903G=	NCBI36
NG_009616.1:g.37966C= , LRG_128:g.37966C=
NG_011734.1:g.711C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478995.2:n.3360C=
ENST00000488970.2:n.3999C=
ENST00000695614.1:c.1843C=	ENSP00000512053.1:p.Arg615=
ENST00000695615.1:c.1843C=	ENSP00000512054.1:p.Arg615=
ENST00000695616.1:c.*1688C=	ENSP00000512055.1:n.*1688C=
ENST00000695617.1:c.1840C=	ENSP00000512056.1:p.Arg614=
ENST00000695618.1:c.*1592C=	ENSP00000512058.1:n.*1592C=
ENST00000695619.1:c.*1553C=	ENSP00000512059.1:n.*1553C=
ENST00000695620.1:c.*1769C=	ENSP00000512060.1:n.*1769C=
ENST00000695621.1:c.*268C=	ENSP00000512061.1:n.*268C=
ENST00000695622.1:c.1780C=	ENSP00000512062.1:p.Arg594=
ENST00000695623.1:c.1837C=	ENSP00000512063.1:p.Arg613=
ENST00000695624.1:n.1148C=
ENST00000695625.1:c.1843C=	ENSP00000512064.1:p.Arg615=
ENST00000695626.1:c.598C=	ENSP00000512065.1:n.598C=
ENST00000695627.1:c.791C=	ENSP00000512066.1:n.791C=
ENST00000695628.1:c.402C=	ENSP00000512067.1:n.402C=
ENST00000695629.1:c.283C=	ENSP00000512068.1:p.Arg95=
ENST00000695630.1:c.570C=
ENST00000695631.1:c.115-11C=
ENST00000703407.1:c.1315C=	ENSP00000512057.1:p.Arg439=
ENST00000308731.8:c.1843C= MANE Select	ENSP00000308176.8:p.Arg615=
ENST00000308731.7:c.1843C=	ENSP00000308176.7:p.Arg615=
ENST00000372880.5:c.1315C=	ENSP00000361971.1:p.Arg439=
ENST00000470069.1:n.208C=
ENST00000618050.4:c.1842C=	ENSP00000479125.1:n.1842C=
ENST00000621635.4:c.1945C=	ENSP00000483570.1:p.Arg649=
NM_000061.2:c.1843C= , LRG_128t1:c.1843C=	NP_000052.1:p.Arg615=
NM_001287344.1:c.1945C=	NP_001274273.1:p.Arg649=
NM_001287345.1:c.1315C=	NP_001274274.1:p.Arg439=
NM_000061.3:c.1843C= MANE Select	NP_000052.1:p.Arg615=
NM_001287344.2:c.1945C=	NP_001274273.1:p.Arg649=
NM_001287345.2:c.1315C=	NP_001274274.1:p.Arg439=