Canonical Allele Identifier: CA413920412

Gene: BTK

Linked Data

• dbSNP Id: rs1926380816
• MyVariant Identifiers: chrX:g.100608909C>T (hg19) ; chrX:g.101353921C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101353921C>T , CM000685.2:g.101353921C>T	GRCh38
NC_000023.10:g.100608909C>T , CM000685.1:g.100608909C>T	GRCh37
NC_000023.9:g.100495565C>T	NCBI36
NG_009616.1:g.37304G>A , LRG_128:g.37304G>A
NG_011734.1:g.49G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478995.2:n.3216G>A
ENST00000488970.2:n.3855G>A
ENST00000695614.1:c.1699G>A	ENSP00000512053.1:p.Glu567Lys
ENST00000695615.1:c.1699G>A	ENSP00000512054.1:p.Glu567Lys
ENST00000695616.1:c.*1544G>A	ENSP00000512055.1:n.*1544G>A
ENST00000695617.1:c.1696G>A	ENSP00000512056.1:p.Glu566Lys
ENST00000695618.1:c.*1448G>A	ENSP00000512058.1:n.*1448G>A
ENST00000695619.1:c.*1409G>A	ENSP00000512059.1:n.*1409G>A
ENST00000695620.1:c.*1625G>A	ENSP00000512060.1:n.*1625G>A
ENST00000695621.1:c.*124G>A	ENSP00000512061.1:n.*124G>A
ENST00000695622.1:c.1636G>A	ENSP00000512062.1:p.Glu546Lys
ENST00000695623.1:c.1693G>A	ENSP00000512063.1:p.Glu565Lys
ENST00000695624.1:n.1004G>A
ENST00000695625.1:c.1699G>A	ENSP00000512064.1:p.Glu567Lys
ENST00000695626.1:c.454G>A	ENSP00000512065.1:n.454G>A
ENST00000695627.1:c.647G>A	ENSP00000512066.1:n.647G>A
ENST00000695628.1:c.258G>A	ENSP00000512067.1:n.258G>A
ENST00000695629.1:c.191-570G>A	ENSP00000512068.1:n.191-570G>A
ENST00000695630.1:c.426G>A
ENST00000695631.1:c.115-673G>A
ENST00000695632.1:n.499G>A
ENST00000703407.1:c.1171G>A	ENSP00000512057.1:p.Glu391Lys
ENST00000308731.8:c.1699G>A MANE Select	ENSP00000308176.8:p.Glu567Lys
ENST00000308731.7:c.1699G>A	ENSP00000308176.7:p.Glu567Lys
ENST00000372880.5:c.1171G>A	ENSP00000361971.1:p.Glu391Lys
ENST00000470069.1:n.64G>A
ENST00000488970.1:n.301G>A
ENST00000618050.4:c.1699G>A	ENSP00000479125.1:p.Glu567Lys
ENST00000621635.4:c.1801G>A	ENSP00000483570.1:p.Glu601Lys
NM_000061.2:c.1699G>A , LRG_128t1:c.1699G>A	NP_000052.1:p.Glu567Lys
NM_001287344.1:c.1801G>A	NP_001274273.1:p.Glu601Lys
NM_001287345.1:c.1171G>A	NP_001274274.1:p.Glu391Lys
NM_000061.3:c.1699G>A MANE Select	NP_000052.1:p.Glu567Lys
NM_001287344.2:c.1801G>A	NP_001274273.1:p.Glu601Lys
NM_001287345.2:c.1171G>A	NP_001274274.1:p.Glu391Lys