Canonical Allele Identifier: CA413918739

Gene: BTK

Linked Data

• MyVariant Identifiers: chrX:g.100608229G>C (hg19) ; chrX:g.101353241G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101353241G>C , CM000685.2:g.101353241G>C	GRCh38
NC_000023.10:g.100608229G>C , CM000685.1:g.100608229G>C	GRCh37
NC_000023.9:g.100494885G>C	NCBI36
NG_009616.1:g.37984C>G , LRG_128:g.37984C>G
NG_011734.1:g.729C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478995.2:n.3378C>G
ENST00000488970.2:n.4017C>G
ENST00000695614.1:c.1861C>G	ENSP00000512053.1:p.Leu621Val
ENST00000695615.1:c.1861C>G	ENSP00000512054.1:p.Leu621Val
ENST00000695616.1:c.*1706C>G	ENSP00000512055.1:n.*1706C>G
ENST00000695617.1:c.1858C>G	ENSP00000512056.1:p.Leu620Val
ENST00000695618.1:c.*1610C>G	ENSP00000512058.1:n.*1610C>G
ENST00000695619.1:c.*1571C>G	ENSP00000512059.1:n.*1571C>G
ENST00000695620.1:c.*1787C>G	ENSP00000512060.1:n.*1787C>G
ENST00000695621.1:c.*286C>G	ENSP00000512061.1:n.*286C>G
ENST00000695622.1:c.1798C>G	ENSP00000512062.1:p.Leu600Val
ENST00000695623.1:c.1855C>G	ENSP00000512063.1:p.Leu619Val
ENST00000695624.1:n.1166C>G
ENST00000695625.1:c.1861C>G	ENSP00000512064.1:p.Leu621Val
ENST00000695626.1:c.616C>G	ENSP00000512065.1:n.616C>G
ENST00000695627.1:c.809C>G	ENSP00000512066.1:n.809C>G
ENST00000695628.1:c.420C>G	ENSP00000512067.1:n.420C>G
ENST00000695629.1:c.301C>G	ENSP00000512068.1:p.Leu101Val
ENST00000695630.1:c.588C>G
ENST00000695631.1:c.122C>G
ENST00000703407.1:c.1333C>G	ENSP00000512057.1:p.Leu445Val
ENST00000308731.8:c.1861C>G MANE Select	ENSP00000308176.8:p.Leu621Val
ENST00000308731.7:c.1861C>G	ENSP00000308176.7:p.Leu621Val
ENST00000372880.5:c.1333C>G	ENSP00000361971.1:p.Leu445Val
ENST00000470069.1:n.226C>G
ENST00000618050.4:c.1860C>G	ENSP00000479125.1:n.1860C>G
ENST00000621635.4:c.1963C>G	ENSP00000483570.1:p.Leu655Val
NM_000061.2:c.1861C>G , LRG_128t1:c.1861C>G	NP_000052.1:p.Leu621Val
NM_001287344.1:c.1963C>G	NP_001274273.1:p.Leu655Val
NM_001287345.1:c.1333C>G	NP_001274274.1:p.Leu445Val
NM_000061.3:c.1861C>G MANE Select	NP_000052.1:p.Leu621Val
NM_001287344.2:c.1963C>G	NP_001274273.1:p.Leu655Val
NM_001287345.2:c.1333C>G	NP_001274274.1:p.Leu445Val