Canonical Allele Identifier: CA413918439

Gene: BTK

Linked Data

• MyVariant Identifiers: chrX:g.100608195C>A (hg19) ; chrX:g.101353207C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101353207C>A , CM000685.2:g.101353207C>A	GRCh38
NC_000023.10:g.100608195C>A , CM000685.1:g.100608195C>A	GRCh37
NC_000023.9:g.100494851C>A	NCBI36
NG_009616.1:g.38018G>T , LRG_128:g.38018G>T
NG_011734.1:g.763G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000478995.2:n.3412G>T
ENST00000488970.2:n.4051G>T
ENST00000695614.1:c.1895G>T	ENSP00000512053.1:p.Ser632Ile
ENST00000695615.1:c.1895G>T	ENSP00000512054.1:p.Ser632Ile
ENST00000695616.1:c.*1740G>T	ENSP00000512055.1:n.*1740G>T
ENST00000695617.1:c.1892G>T	ENSP00000512056.1:p.Ser631Ile
ENST00000695618.1:c.*1644G>T	ENSP00000512058.1:n.*1644G>T
ENST00000695619.1:c.*1605G>T	ENSP00000512059.1:n.*1605G>T
ENST00000695620.1:c.*1821G>T	ENSP00000512060.1:n.*1821G>T
ENST00000695621.1:c.*320G>T	ENSP00000512061.1:n.*320G>T
ENST00000695622.1:c.1832G>T	ENSP00000512062.1:p.Ser611Ile
ENST00000695623.1:c.1889G>T	ENSP00000512063.1:p.Ser630Ile
ENST00000695624.1:n.1200G>T
ENST00000695625.1:c.1875+20G>T	ENSP00000512064.1:n.1875+20G>T
ENST00000695626.1:c.650G>T	ENSP00000512065.1:n.650G>T
ENST00000695627.1:c.843G>T	ENSP00000512066.1:n.843G>T
ENST00000695628.1:c.454G>T	ENSP00000512067.1:n.454G>T
ENST00000695629.1:c.335G>T	ENSP00000512068.1:p.Ser112Ile
ENST00000695630.1:c.622G>T
ENST00000695631.1:c.156G>T
ENST00000703407.1:c.1367G>T	ENSP00000512057.1:p.Ser456Ile
ENST00000308731.8:c.1895G>T MANE Select	ENSP00000308176.8:p.Ser632Ile
ENST00000308731.7:c.1895G>T	ENSP00000308176.7:p.Ser632Ile
ENST00000372880.5:c.1367G>T	ENSP00000361971.1:p.Ser456Ile
ENST00000470069.1:n.260G>T
ENST00000618050.4:c.1894G>T	ENSP00000479125.1:n.1894G>T
ENST00000621635.4:c.1997G>T	ENSP00000483570.1:p.Ser666Ile
NM_000061.2:c.1895G>T , LRG_128t1:c.1895G>T	NP_000052.1:p.Ser632Ile
NM_001287344.1:c.1997G>T	NP_001274273.1:p.Ser666Ile
NM_001287345.1:c.1367G>T	NP_001274274.1:p.Ser456Ile
NM_000061.3:c.1895G>T MANE Select	NP_000052.1:p.Ser632Ile
NM_001287344.2:c.1997G>T	NP_001274273.1:p.Ser666Ile
NM_001287345.2:c.1367G>T	NP_001274274.1:p.Ser456Ile