Canonical Allele Identifier: CA413924927

Gene: BTK

Linked Data

• MyVariant Identifiers: chrX:g.100611805T>A (hg19) ; chrX:g.101356817T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101356817T>A , CM000685.2:g.101356817T>A	GRCh38
NC_000023.10:g.100611805T>A , CM000685.1:g.100611805T>A	GRCh37
NC_000023.9:g.100498461T>A	NCBI36
NG_009616.1:g.34408A>T , LRG_128:g.34408A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478995.2:n.1476A>T
ENST00000488970.2:n.1474A>T
ENST00000695614.1:c.1316A>T	ENSP00000512053.1:p.Glu439Val
ENST00000695615.1:c.1316A>T	ENSP00000512054.1:p.Glu439Val
ENST00000695616.1:c.*1161A>T	ENSP00000512055.1:n.*1161A>T
ENST00000695617.1:c.1313A>T	ENSP00000512056.1:p.Glu438Val
ENST00000695618.1:c.*1065A>T	ENSP00000512058.1:n.*1065A>T
ENST00000695619.1:c.*1026A>T	ENSP00000512059.1:n.*1026A>T
ENST00000695620.1:c.*1161A>T	ENSP00000512060.1:n.*1161A>T
ENST00000695621.1:c.1316A>T	ENSP00000512061.1:p.Glu439Val
ENST00000695622.1:c.1253A>T	ENSP00000512062.1:p.Glu418Val
ENST00000695623.1:c.1310A>T	ENSP00000512063.1:p.Glu437Val
ENST00000695624.1:n.621A>T
ENST00000695625.1:c.1316A>T	ENSP00000512064.1:p.Glu439Val
ENST00000695626.1:c.288A>T	ENSP00000512065.1:p.Ter96Cys
ENST00000695627.1:c.329A>T	ENSP00000512066.1:p.Glu110Val
ENST00000695628.1:c.190+692A>T	ENSP00000512067.1:n.190+692A>T
ENST00000695629.1:c.190+692A>T	ENSP00000512068.1:n.190+692A>T
ENST00000695630.1:c.325A>T
ENST00000695631.1:c.114+1493A>T
ENST00000695632.1:n.333A>T
ENST00000703407.1:c.1038+1557A>T	ENSP00000512057.1:n.1038+1557A>T
ENST00000308731.8:c.1316A>T MANE Select	ENSP00000308176.8:p.Glu439Val
ENST00000308731.7:c.1316A>T	ENSP00000308176.7:p.Glu439Val
ENST00000372880.5:c.1038+1557A>T	ENSP00000361971.1:n.1038+1557A>T
ENST00000470329.1:n.266A>T
ENST00000618050.4:c.1316A>T	ENSP00000479125.1:p.Glu439Val
ENST00000621635.4:c.1418A>T	ENSP00000483570.1:p.Glu473Val
NM_000061.2:c.1316A>T , LRG_128t1:c.1316A>T	NP_000052.1:p.Glu439Val
NM_001287344.1:c.1418A>T	NP_001274273.1:p.Glu473Val
NM_001287345.1:c.1038+1557A>T	NP_001274274.1:n.1038+1557A>T
NM_000061.3:c.1316A>T MANE Select	NP_000052.1:p.Glu439Val
NM_001287344.2:c.1418A>T	NP_001274273.1:p.Glu473Val
NM_001287345.2:c.1038+1557A>T	NP_001274274.1:n.1038+1557A>T