Canonical Allele Identifier: CA2448284772

Gene: BTK

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101359274C= , CM000685.2:g.101359274C=	GRCh38
NC_000023.10:g.100614262C= , CM000685.1:g.100614262C=	GRCh37
NC_000023.9:g.100500918C=	NCBI36
NG_009616.1:g.31951G= , LRG_128:g.31951G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000464006.2:n.674+19G=
ENST00000478995.2:n.1054+19G=
ENST00000488970.2:n.1052+19G=
ENST00000695614.1:c.894+19G=	ENSP00000512053.1:n.894+19G=
ENST00000695615.1:c.894+19G=	ENSP00000512054.1:n.894+19G=
ENST00000695616.1:c.*739+19G=	ENSP00000512055.1:n.*739+19G=
ENST00000695617.1:c.891+19G=	ENSP00000512056.1:n.891+19G=
ENST00000695618.1:c.*643+19G=	ENSP00000512058.1:n.*643+19G=
ENST00000695619.1:c.*684+814G=	ENSP00000512059.1:n.*684+814G=
ENST00000695620.1:c.*739+19G=	ENSP00000512060.1:n.*739+19G=
ENST00000695621.1:c.894+19G=	ENSP00000512061.1:n.894+19G=
ENST00000695622.1:c.831+19G=	ENSP00000512062.1:n.831+19G=
ENST00000695623.1:c.888+19G=	ENSP00000512063.1:n.888+19G=
ENST00000695624.1:n.199+19G=
ENST00000695625.1:c.894+19G=	ENSP00000512064.1:n.894+19G=
ENST00000703407.1:c.894+19G=	ENSP00000512057.1:n.894+19G=
ENST00000308731.8:c.894+19G= MANE Select	ENSP00000308176.8:n.894+19G=
ENST00000308731.7:c.894+19G=	ENSP00000308176.7:n.894+19G=
ENST00000372880.5:c.894+19G=	ENSP00000361971.1:n.894+19G=
ENST00000618050.4:c.894+19G=	ENSP00000479125.1:n.894+19G=
ENST00000621635.4:c.996+19G=	ENSP00000483570.1:n.996+19G=
NM_000061.2:c.894+19G= , LRG_128t1:c.894+19G=	NP_000052.1:n.894+19G=
NM_001287344.1:c.996+19G=	NP_001274273.1:n.996+19G=
NM_001287345.1:c.894+19G=	NP_001274274.1:n.894+19G=
NM_000061.3:c.894+19G= MANE Select	NP_000052.1:n.894+19G=
NM_001287344.2:c.996+19G=	NP_001274273.1:n.996+19G=
NM_001287345.2:c.894+19G=	NP_001274274.1:n.894+19G=