Canonical Allele Identifier: CA413923035

Gene: BTK

Linked Data

• MyVariant Identifiers: chrX:g.100611055G>C (hg19) ; chrX:g.101356067G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101356067G>C , CM000685.2:g.101356067G>C	GRCh38
NC_000023.10:g.100611055G>C , CM000685.1:g.100611055G>C	GRCh37
NC_000023.9:g.100497711G>C	NCBI36
NG_009616.1:g.35158C>G , LRG_128:g.35158C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000478995.2:n.1711C>G
ENST00000488970.2:n.1709C>G
ENST00000695614.1:c.1551C>G	ENSP00000512053.1:p.Phe517Leu
ENST00000695615.1:c.1551C>G	ENSP00000512054.1:p.Phe517Leu
ENST00000695616.1:c.*1396C>G	ENSP00000512055.1:n.*1396C>G
ENST00000695617.1:c.1548C>G	ENSP00000512056.1:p.Phe516Leu
ENST00000695618.1:c.*1300C>G	ENSP00000512058.1:n.*1300C>G
ENST00000695619.1:c.*1261C>G	ENSP00000512059.1:n.*1261C>G
ENST00000695620.1:c.*1477C>G	ENSP00000512060.1:n.*1477C>G
ENST00000695621.1:c.1551C>G	ENSP00000512061.1:p.Phe517Leu
ENST00000695622.1:c.1488C>G	ENSP00000512062.1:p.Phe496Leu
ENST00000695623.1:c.1545C>G	ENSP00000512063.1:p.Phe515Leu
ENST00000695624.1:n.856C>G
ENST00000695625.1:c.1551C>G	ENSP00000512064.1:p.Phe517Leu
ENST00000695626.1:c.321+717C>G	ENSP00000512065.1:n.321+717C>G
ENST00000695627.1:c.564C>G	ENSP00000512066.1:p.Phe188Leu
ENST00000695628.1:c.190+1442C>G	ENSP00000512067.1:n.190+1442C>G
ENST00000695629.1:c.190+1442C>G	ENSP00000512068.1:n.190+1442C>G
ENST00000695630.1:c.358+717C>G
ENST00000695631.1:c.114+2243C>G
ENST00000695632.1:n.366+717C>G
ENST00000703407.1:c.1039-1373C>G	ENSP00000512057.1:n.1039-1373C>G
ENST00000308731.8:c.1551C>G MANE Select	ENSP00000308176.8:p.Phe517Leu
ENST00000308731.7:c.1551C>G	ENSP00000308176.7:p.Phe517Leu
ENST00000372880.5:c.1039-1373C>G	ENSP00000361971.1:n.1039-1373C>G
ENST00000478995.1:n.223C>G
ENST00000618050.4:c.1551C>G	ENSP00000479125.1:p.Phe517Leu
ENST00000621635.4:c.1653C>G	ENSP00000483570.1:p.Phe551Leu
NM_000061.2:c.1551C>G , LRG_128t1:c.1551C>G	NP_000052.1:p.Phe517Leu
NM_001287344.1:c.1653C>G	NP_001274273.1:p.Phe551Leu
NM_001287345.1:c.1039-1373C>G	NP_001274274.1:n.1039-1373C>G
NM_000061.3:c.1551C>G MANE Select	NP_000052.1:p.Phe517Leu
NM_001287344.2:c.1653C>G	NP_001274273.1:p.Phe551Leu
NM_001287345.2:c.1039-1373C>G	NP_001274274.1:n.1039-1373C>G