Canonical Allele Identifier: CA517532182

Gene: BTK

Linked Data

• MyVariant Identifiers: chrX:g.100611121A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101356133A>T , CM000685.2:g.101356133A>T	GRCh38
NC_000023.10:g.100611121A>T , CM000685.1:g.100611121A>T	GRCh37
NC_000023.9:g.100497777A>T	NCBI36
NG_009616.1:g.35092T>A , LRG_128:g.35092T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478995.2:n.1645T>A
ENST00000488970.2:n.1643T>A
ENST00000695614.1:c.1485T>A	ENSP00000512053.1:p.Thr495=
ENST00000695615.1:c.1485T>A	ENSP00000512054.1:p.Thr495=
ENST00000695616.1:c.*1330T>A	ENSP00000512055.1:n.*1330T>A
ENST00000695617.1:c.1482T>A	ENSP00000512056.1:p.Thr494=
ENST00000695618.1:c.*1234T>A	ENSP00000512058.1:n.*1234T>A
ENST00000695619.1:c.*1195T>A	ENSP00000512059.1:n.*1195T>A
ENST00000695620.1:c.*1411T>A	ENSP00000512060.1:n.*1411T>A
ENST00000695621.1:c.1485T>A	ENSP00000512061.1:p.Thr495=
ENST00000695622.1:c.1422T>A	ENSP00000512062.1:p.Thr474=
ENST00000695623.1:c.1479T>A	ENSP00000512063.1:p.Thr493=
ENST00000695624.1:n.790T>A
ENST00000695625.1:c.1485T>A	ENSP00000512064.1:p.Thr495=
ENST00000695626.1:c.321+651T>A	ENSP00000512065.1:n.321+651T>A
ENST00000695627.1:c.498T>A	ENSP00000512066.1:p.Thr166=
ENST00000695628.1:c.190+1376T>A	ENSP00000512067.1:n.190+1376T>A
ENST00000695629.1:c.190+1376T>A	ENSP00000512068.1:n.190+1376T>A
ENST00000695630.1:c.358+651T>A
ENST00000695631.1:c.114+2177T>A
ENST00000695632.1:n.366+651T>A
ENST00000703407.1:c.1039-1439T>A	ENSP00000512057.1:n.1039-1439T>A
ENST00000308731.8:c.1485T>A MANE Select	ENSP00000308176.8:p.Thr495=
ENST00000308731.7:c.1485T>A	ENSP00000308176.7:p.Thr495=
ENST00000372880.5:c.1039-1439T>A	ENSP00000361971.1:n.1039-1439T>A
ENST00000478995.1:n.157T>A
ENST00000618050.4:c.1485T>A	ENSP00000479125.1:p.Thr495=
ENST00000621635.4:c.1587T>A	ENSP00000483570.1:p.Thr529=
NM_000061.2:c.1485T>A , LRG_128t1:c.1485T>A	NP_000052.1:p.Thr495=
NM_001287344.1:c.1587T>A	NP_001274273.1:p.Thr529=
NM_001287345.1:c.1039-1439T>A	NP_001274274.1:n.1039-1439T>A
NM_000061.3:c.1485T>A MANE Select	NP_000052.1:p.Thr495=
NM_001287344.2:c.1587T>A	NP_001274273.1:p.Thr529=
NM_001287345.2:c.1039-1439T>A	NP_001274274.1:n.1039-1439T>A