Canonical Allele Identifier: CA413925078

Gene: BTK

Linked Data

• MyVariant Identifiers: chrX:g.100611836T>C (hg19) ; chrX:g.101356848T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101356848T>C , CM000685.2:g.101356848T>C	GRCh38
NC_000023.10:g.100611836T>C , CM000685.1:g.100611836T>C	GRCh37
NC_000023.9:g.100498492T>C	NCBI36
NG_009616.1:g.34377A>G , LRG_128:g.34377A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000478995.2:n.1445A>G
ENST00000488970.2:n.1443A>G
ENST00000695614.1:c.1285A>G	ENSP00000512053.1:p.Ile429Val
ENST00000695615.1:c.1285A>G	ENSP00000512054.1:p.Ile429Val
ENST00000695616.1:c.*1130A>G	ENSP00000512055.1:n.*1130A>G
ENST00000695617.1:c.1282A>G	ENSP00000512056.1:p.Ile428Val
ENST00000695618.1:c.*1034A>G	ENSP00000512058.1:n.*1034A>G
ENST00000695619.1:c.*995A>G	ENSP00000512059.1:n.*995A>G
ENST00000695620.1:c.*1130A>G	ENSP00000512060.1:n.*1130A>G
ENST00000695621.1:c.1285A>G	ENSP00000512061.1:p.Ile429Val
ENST00000695622.1:c.1222A>G	ENSP00000512062.1:p.Ile408Val
ENST00000695623.1:c.1279A>G	ENSP00000512063.1:p.Ile427Val
ENST00000695624.1:n.590A>G
ENST00000695625.1:c.1285A>G	ENSP00000512064.1:p.Ile429Val
ENST00000695626.1:c.257A>G	ENSP00000512065.1:p.His86Arg
ENST00000695627.1:c.298A>G	ENSP00000512066.1:p.Ile100Val
ENST00000695628.1:c.190+661A>G	ENSP00000512067.1:n.190+661A>G
ENST00000695629.1:c.190+661A>G	ENSP00000512068.1:n.190+661A>G
ENST00000695630.1:c.294A>G
ENST00000695631.1:c.114+1462A>G
ENST00000695632.1:n.302A>G
ENST00000703407.1:c.1038+1526A>G	ENSP00000512057.1:n.1038+1526A>G
ENST00000308731.8:c.1285A>G MANE Select	ENSP00000308176.8:p.Ile429Val
ENST00000308731.7:c.1285A>G	ENSP00000308176.7:p.Ile429Val
ENST00000372880.5:c.1038+1526A>G	ENSP00000361971.1:n.1038+1526A>G
ENST00000470329.1:n.235A>G
ENST00000618050.4:c.1285A>G	ENSP00000479125.1:p.Ile429Val
ENST00000621635.4:c.1387A>G	ENSP00000483570.1:p.Ile463Val
NM_000061.2:c.1285A>G , LRG_128t1:c.1285A>G	NP_000052.1:p.Ile429Val
NM_001287344.1:c.1387A>G	NP_001274273.1:p.Ile463Val
NM_001287345.1:c.1038+1526A>G	NP_001274274.1:n.1038+1526A>G
NM_000061.3:c.1285A>G MANE Select	NP_000052.1:p.Ile429Val
NM_001287344.2:c.1387A>G	NP_001274273.1:p.Ile463Val
NM_001287345.2:c.1038+1526A>G	NP_001274274.1:n.1038+1526A>G