Canonical Allele Identifier: CA2448284027
Gene: BTK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101356136C= , CM000685.2:g.101356136C= GRCh38
NC_000023.10:g.100611124C= , CM000685.1:g.100611124C= GRCh37
NC_000023.9:g.100497780C= NCBI36
NG_009616.1:g.35089G= , LRG_128:g.35089G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000478995.2:n.1642G=
ENST00000488970.2:n.1640G=
ENST00000695614.1:c.1482G= ENSP00000512053.1:p.Gln494=
ENST00000695615.1:c.1482G= ENSP00000512054.1:p.Gln494=
ENST00000695616.1:c.*1327G= ENSP00000512055.1:n.*1327G=
ENST00000695617.1:c.1479G= ENSP00000512056.1:p.Gln493=
ENST00000695618.1:c.*1231G= ENSP00000512058.1:n.*1231G=
ENST00000695619.1:c.*1192G= ENSP00000512059.1:n.*1192G=
ENST00000695620.1:c.*1408G= ENSP00000512060.1:n.*1408G=
ENST00000695621.1:c.1482G= ENSP00000512061.1:p.Gln494=
ENST00000695622.1:c.1419G= ENSP00000512062.1:p.Gln473=
ENST00000695623.1:c.1476G= ENSP00000512063.1:p.Gln492=
ENST00000695624.1:n.787G=
ENST00000695625.1:c.1482G= ENSP00000512064.1:p.Gln494=
ENST00000695626.1:c.321+648G= ENSP00000512065.1:n.321+648G=
ENST00000695627.1:c.495G= ENSP00000512066.1:p.Gln165=
ENST00000695628.1:c.190+1373G= ENSP00000512067.1:n.190+1373G=
ENST00000695629.1:c.190+1373G= ENSP00000512068.1:n.190+1373G=
ENST00000695630.1:c.358+648G=
ENST00000695631.1:c.114+2174G=
ENST00000695632.1:n.366+648G=
ENST00000703407.1:c.1039-1442G= ENSP00000512057.1:n.1039-1442G=
ENST00000308731.8:c.1482G= MANE Select ENSP00000308176.8:p.Gln494=
ENST00000308731.7:c.1482G= ENSP00000308176.7:p.Gln494=
ENST00000372880.5:c.1039-1442G= ENSP00000361971.1:n.1039-1442G=
ENST00000478995.1:n.154G=
ENST00000618050.4:c.1482G= ENSP00000479125.1:p.Gln494=
ENST00000621635.4:c.1584G= ENSP00000483570.1:p.Gln528=
NM_000061.2:c.1482G= , LRG_128t1:c.1482G= NP_000052.1:p.Gln494=
NM_001287344.1:c.1584G= NP_001274273.1:p.Gln528=
NM_001287345.1:c.1039-1442G= NP_001274274.1:n.1039-1442G=
NM_000061.3:c.1482G= MANE Select NP_000052.1:p.Gln494=
NM_001287344.2:c.1584G= NP_001274273.1:p.Gln528=
NM_001287345.2:c.1039-1442G= NP_001274274.1:n.1039-1442G=