Canonical Allele Identifier: CA2448283033

Gene: BTK

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101353264C= , CM000685.2:g.101353264C=	GRCh38
NC_000023.10:g.100608252C= , CM000685.1:g.100608252C=	GRCh37
NC_000023.9:g.100494908C=	NCBI36
NG_009616.1:g.37961G= , LRG_128:g.37961G=
NG_011734.1:g.706G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478995.2:n.3355G=
ENST00000488970.2:n.3994G=
ENST00000695614.1:c.1838G=	ENSP00000512053.1:p.Gly613=
ENST00000695615.1:c.1838G=	ENSP00000512054.1:p.Gly613=
ENST00000695616.1:c.*1683G=	ENSP00000512055.1:n.*1683G=
ENST00000695617.1:c.1835G=	ENSP00000512056.1:p.Gly612=
ENST00000695618.1:c.*1587G=	ENSP00000512058.1:n.*1587G=
ENST00000695619.1:c.*1548G=	ENSP00000512059.1:n.*1548G=
ENST00000695620.1:c.*1764G=	ENSP00000512060.1:n.*1764G=
ENST00000695621.1:c.*263G=	ENSP00000512061.1:n.*263G=
ENST00000695622.1:c.1775G=	ENSP00000512062.1:p.Gly592=
ENST00000695623.1:c.1832G=	ENSP00000512063.1:p.Gly611=
ENST00000695624.1:n.1143G=
ENST00000695625.1:c.1838G=	ENSP00000512064.1:p.Gly613=
ENST00000695626.1:c.593G=	ENSP00000512065.1:n.593G=
ENST00000695627.1:c.786G=	ENSP00000512066.1:n.786G=
ENST00000695628.1:c.397G=	ENSP00000512067.1:n.397G=
ENST00000695629.1:c.278G=	ENSP00000512068.1:p.Gly93=
ENST00000695630.1:c.565G=
ENST00000695631.1:c.115-16G=
ENST00000703407.1:c.1310G=	ENSP00000512057.1:p.Gly437=
ENST00000308731.8:c.1838G= MANE Select	ENSP00000308176.8:p.Gly613=
ENST00000308731.7:c.1838G=	ENSP00000308176.7:p.Gly613=
ENST00000372880.5:c.1310G=	ENSP00000361971.1:p.Gly437=
ENST00000470069.1:n.203G=
ENST00000618050.4:c.1837G=	ENSP00000479125.1:n.1837G=
ENST00000621635.4:c.1940G=	ENSP00000483570.1:p.Gly647=
NM_000061.2:c.1838G= , LRG_128t1:c.1838G=	NP_000052.1:p.Gly613=
NM_001287344.1:c.1940G=	NP_001274273.1:p.Gly647=
NM_001287345.1:c.1310G=	NP_001274274.1:p.Gly437=
NM_000061.3:c.1838G= MANE Select	NP_000052.1:p.Gly613=
NM_001287344.2:c.1940G=	NP_001274273.1:p.Gly647=
NM_001287345.2:c.1310G=	NP_001274274.1:p.Gly437=