Canonical Allele Identifier: CA2448283026

Gene: BTK

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101353242A= , CM000685.2:g.101353242A=	GRCh38
NC_000023.10:g.100608230A= , CM000685.1:g.100608230A=	GRCh37
NC_000023.9:g.100494886A=	NCBI36
NG_009616.1:g.37983T= , LRG_128:g.37983T=
NG_011734.1:g.728T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478995.2:n.3377T=
ENST00000488970.2:n.4016T=
ENST00000695614.1:c.1860T=	ENSP00000512053.1:p.His620=
ENST00000695615.1:c.1860T=	ENSP00000512054.1:p.His620=
ENST00000695616.1:c.*1705T=	ENSP00000512055.1:n.*1705T=
ENST00000695617.1:c.1857T=	ENSP00000512056.1:p.His619=
ENST00000695618.1:c.*1609T=	ENSP00000512058.1:n.*1609T=
ENST00000695619.1:c.*1570T=	ENSP00000512059.1:n.*1570T=
ENST00000695620.1:c.*1786T=	ENSP00000512060.1:n.*1786T=
ENST00000695621.1:c.*285T=	ENSP00000512061.1:n.*285T=
ENST00000695622.1:c.1797T=	ENSP00000512062.1:p.His599=
ENST00000695623.1:c.1854T=	ENSP00000512063.1:p.His618=
ENST00000695624.1:n.1165T=
ENST00000695625.1:c.1860T=	ENSP00000512064.1:p.His620=
ENST00000695626.1:c.615T=	ENSP00000512065.1:n.615T=
ENST00000695627.1:c.808T=	ENSP00000512066.1:n.808T=
ENST00000695628.1:c.419T=	ENSP00000512067.1:n.419T=
ENST00000695629.1:c.300T=	ENSP00000512068.1:p.His100=
ENST00000695630.1:c.587T=
ENST00000695631.1:c.121T=
ENST00000703407.1:c.1332T=	ENSP00000512057.1:p.His444=
ENST00000308731.8:c.1860T= MANE Select	ENSP00000308176.8:p.His620=
ENST00000308731.7:c.1860T=	ENSP00000308176.7:p.His620=
ENST00000372880.5:c.1332T=	ENSP00000361971.1:p.His444=
ENST00000470069.1:n.225T=
ENST00000618050.4:c.1859T=	ENSP00000479125.1:n.1859T=
ENST00000621635.4:c.1962T=	ENSP00000483570.1:p.His654=
NM_000061.2:c.1860T= , LRG_128t1:c.1860T=	NP_000052.1:p.His620=
NM_001287344.1:c.1962T=	NP_001274273.1:p.His654=
NM_001287345.1:c.1332T=	NP_001274274.1:p.His444=
NM_000061.3:c.1860T= MANE Select	NP_000052.1:p.His620=
NM_001287344.2:c.1962T=	NP_001274273.1:p.His654=
NM_001287345.2:c.1332T=	NP_001274274.1:p.His444=