Canonical Allele Identifier: CA413918712

Gene: BTK

Linked Data

• MyVariant Identifiers: chrX:g.100608223A>T (hg19) ; chrX:g.101353235A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101353235A>T , CM000685.2:g.101353235A>T	GRCh38
NC_000023.10:g.100608223A>T , CM000685.1:g.100608223A>T	GRCh37
NC_000023.9:g.100494879A>T	NCBI36
NG_009616.1:g.37990T>A , LRG_128:g.37990T>A
NG_011734.1:g.735T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478995.2:n.3384T>A
ENST00000488970.2:n.4023T>A
ENST00000695614.1:c.1867T>A	ENSP00000512053.1:p.Ser623Thr
ENST00000695615.1:c.1867T>A	ENSP00000512054.1:p.Ser623Thr
ENST00000695616.1:c.*1712T>A	ENSP00000512055.1:n.*1712T>A
ENST00000695617.1:c.1864T>A	ENSP00000512056.1:p.Ser622Thr
ENST00000695618.1:c.*1616T>A	ENSP00000512058.1:n.*1616T>A
ENST00000695619.1:c.*1577T>A	ENSP00000512059.1:n.*1577T>A
ENST00000695620.1:c.*1793T>A	ENSP00000512060.1:n.*1793T>A
ENST00000695621.1:c.*292T>A	ENSP00000512061.1:n.*292T>A
ENST00000695622.1:c.1804T>A	ENSP00000512062.1:p.Ser602Thr
ENST00000695623.1:c.1861T>A	ENSP00000512063.1:p.Ser621Thr
ENST00000695624.1:n.1172T>A
ENST00000695625.1:c.1867T>A	ENSP00000512064.1:p.Ser623Thr
ENST00000695626.1:c.622T>A	ENSP00000512065.1:n.622T>A
ENST00000695627.1:c.815T>A	ENSP00000512066.1:n.815T>A
ENST00000695628.1:c.426T>A	ENSP00000512067.1:n.426T>A
ENST00000695629.1:c.307T>A	ENSP00000512068.1:p.Ser103Thr
ENST00000695630.1:c.594T>A
ENST00000695631.1:c.128T>A
ENST00000703407.1:c.1339T>A	ENSP00000512057.1:p.Ser447Thr
ENST00000308731.8:c.1867T>A MANE Select	ENSP00000308176.8:p.Ser623Thr
ENST00000308731.7:c.1867T>A	ENSP00000308176.7:p.Ser623Thr
ENST00000372880.5:c.1339T>A	ENSP00000361971.1:p.Ser447Thr
ENST00000470069.1:n.232T>A
ENST00000618050.4:c.1866T>A	ENSP00000479125.1:n.1866T>A
ENST00000621635.4:c.1969T>A	ENSP00000483570.1:p.Ser657Thr
NM_000061.2:c.1867T>A , LRG_128t1:c.1867T>A	NP_000052.1:p.Ser623Thr
NM_001287344.1:c.1969T>A	NP_001274273.1:p.Ser657Thr
NM_001287345.1:c.1339T>A	NP_001274274.1:p.Ser447Thr
NM_000061.3:c.1867T>A MANE Select	NP_000052.1:p.Ser623Thr
NM_001287344.2:c.1969T>A	NP_001274273.1:p.Ser657Thr
NM_001287345.2:c.1339T>A	NP_001274274.1:p.Ser447Thr