Canonical Allele Identifier: CA413925965

Gene: BTK

Linked Data

• MyVariant Identifiers: chrX:g.100612499T>C (hg19) ; chrX:g.101357511T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101357511T>C , CM000685.2:g.101357511T>C	GRCh38
NC_000023.10:g.100612499T>C , CM000685.1:g.100612499T>C	GRCh37
NC_000023.9:g.100499155T>C	NCBI36
NG_009616.1:g.33714A>G , LRG_128:g.33714A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000478995.2:n.1335A>G
ENST00000488970.2:n.1333A>G
ENST00000695614.1:c.1175A>G	ENSP00000512053.1:p.Tyr392Cys
ENST00000695615.1:c.1175A>G	ENSP00000512054.1:p.Tyr392Cys
ENST00000695616.1:c.*1020A>G	ENSP00000512055.1:n.*1020A>G
ENST00000695617.1:c.1172A>G	ENSP00000512056.1:p.Tyr391Cys
ENST00000695618.1:c.*924A>G	ENSP00000512058.1:n.*924A>G
ENST00000695619.1:c.*885A>G	ENSP00000512059.1:n.*885A>G
ENST00000695620.1:c.*1020A>G	ENSP00000512060.1:n.*1020A>G
ENST00000695621.1:c.1175A>G	ENSP00000512061.1:p.Tyr392Cys
ENST00000695622.1:c.1112A>G	ENSP00000512062.1:p.Tyr371Cys
ENST00000695623.1:c.1169A>G	ENSP00000512063.1:p.Tyr390Cys
ENST00000695624.1:n.480A>G
ENST00000695625.1:c.1175A>G	ENSP00000512064.1:p.Tyr392Cys
ENST00000695626.1:c.188A>G	ENSP00000512065.1:p.Tyr63Cys
ENST00000695627.1:c.188A>G	ENSP00000512066.1:p.Tyr63Cys
ENST00000695628.1:c.188A>G	ENSP00000512067.1:p.Tyr63Cys
ENST00000695629.1:c.188A>G	ENSP00000512068.1:p.Tyr63Cys
ENST00000695630.1:c.184A>G
ENST00000695631.1:c.114+799A>G
ENST00000695632.1:n.192A>G
ENST00000703407.1:c.1038+863A>G	ENSP00000512057.1:n.1038+863A>G
ENST00000308731.8:c.1175A>G MANE Select	ENSP00000308176.8:p.Tyr392Cys
ENST00000308731.7:c.1175A>G	ENSP00000308176.7:p.Tyr392Cys
ENST00000372880.5:c.1038+863A>G	ENSP00000361971.1:n.1038+863A>G
ENST00000470329.1:n.125A>G
ENST00000618050.4:c.1175A>G	ENSP00000479125.1:p.Tyr392Cys
ENST00000621635.4:c.1277A>G	ENSP00000483570.1:p.Tyr426Cys
NM_000061.2:c.1175A>G , LRG_128t1:c.1175A>G	NP_000052.1:p.Tyr392Cys
NM_001287344.1:c.1277A>G	NP_001274273.1:p.Tyr426Cys
NM_001287345.1:c.1038+863A>G	NP_001274274.1:n.1038+863A>G
NM_000061.3:c.1175A>G MANE Select	NP_000052.1:p.Tyr392Cys
NM_001287344.2:c.1277A>G	NP_001274273.1:p.Tyr426Cys
NM_001287345.2:c.1038+863A>G	NP_001274274.1:n.1038+863A>G