Canonical Allele Identifier: CA413918606

Gene: BTK

Linked Data

• MyVariant Identifiers: chrX:g.100608211A>C (hg19) ; chrX:g.101353223A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101353223A>C , CM000685.2:g.101353223A>C	GRCh38
NC_000023.10:g.100608211A>C , CM000685.1:g.100608211A>C	GRCh37
NC_000023.9:g.100494867A>C	NCBI36
NG_009616.1:g.38002T>G , LRG_128:g.38002T>G
NG_011734.1:g.747T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478995.2:n.3396T>G
ENST00000488970.2:n.4035T>G
ENST00000695614.1:c.1879T>G	ENSP00000512053.1:p.Tyr627Asp
ENST00000695615.1:c.1879T>G	ENSP00000512054.1:p.Tyr627Asp
ENST00000695616.1:c.*1724T>G	ENSP00000512055.1:n.*1724T>G
ENST00000695617.1:c.1876T>G	ENSP00000512056.1:p.Tyr626Asp
ENST00000695618.1:c.*1628T>G	ENSP00000512058.1:n.*1628T>G
ENST00000695619.1:c.*1589T>G	ENSP00000512059.1:n.*1589T>G
ENST00000695620.1:c.*1805T>G	ENSP00000512060.1:n.*1805T>G
ENST00000695621.1:c.*304T>G	ENSP00000512061.1:n.*304T>G
ENST00000695622.1:c.1816T>G	ENSP00000512062.1:p.Tyr606Asp
ENST00000695623.1:c.1873T>G	ENSP00000512063.1:p.Tyr625Asp
ENST00000695624.1:n.1184T>G
ENST00000695625.1:c.1875+4T>G	ENSP00000512064.1:n.1875+4T>G
ENST00000695626.1:c.634T>G	ENSP00000512065.1:n.634T>G
ENST00000695627.1:c.827T>G	ENSP00000512066.1:n.827T>G
ENST00000695628.1:c.438T>G	ENSP00000512067.1:n.438T>G
ENST00000695629.1:c.319T>G	ENSP00000512068.1:p.Tyr107Asp
ENST00000695630.1:c.606T>G
ENST00000695631.1:c.140T>G
ENST00000703407.1:c.1351T>G	ENSP00000512057.1:p.Tyr451Asp
ENST00000308731.8:c.1879T>G MANE Select	ENSP00000308176.8:p.Tyr627Asp
ENST00000308731.7:c.1879T>G	ENSP00000308176.7:p.Tyr627Asp
ENST00000372880.5:c.1351T>G	ENSP00000361971.1:p.Tyr451Asp
ENST00000470069.1:n.244T>G
ENST00000618050.4:c.1878T>G	ENSP00000479125.1:n.1878T>G
ENST00000621635.4:c.1981T>G	ENSP00000483570.1:p.Tyr661Asp
NM_000061.2:c.1879T>G , LRG_128t1:c.1879T>G	NP_000052.1:p.Tyr627Asp
NM_001287344.1:c.1981T>G	NP_001274273.1:p.Tyr661Asp
NM_001287345.1:c.1351T>G	NP_001274274.1:p.Tyr451Asp
NM_000061.3:c.1879T>G MANE Select	NP_000052.1:p.Tyr627Asp
NM_001287344.2:c.1981T>G	NP_001274273.1:p.Tyr661Asp
NM_001287345.2:c.1351T>G	NP_001274274.1:p.Tyr451Asp