Canonical Allele Identifier: CA2822688522

Gene: BTK

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101353744G>A , CM000685.2:g.101353744G>A	GRCh38
NC_000023.10:g.100608732G>A , CM000685.1:g.100608732G>A	GRCh37
NC_000023.9:g.100495388G>A	NCBI36
NG_009616.1:g.37481C>T , LRG_128:g.37481C>T
NG_011734.1:g.226C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478995.2:n.3267+126C>T
ENST00000488970.2:n.3906+126C>T
ENST00000695614.1:c.1750+126C>T	ENSP00000512053.1:n.1750+126C>T
ENST00000695615.1:c.1750+126C>T	ENSP00000512054.1:n.1750+126C>T
ENST00000695616.1:c.*1595+126C>T	ENSP00000512055.1:n.*1595+126C>T
ENST00000695617.1:c.1747+126C>T	ENSP00000512056.1:n.1747+126C>T
ENST00000695618.1:c.*1499+126C>T	ENSP00000512058.1:n.*1499+126C>T
ENST00000695619.1:c.*1460+126C>T	ENSP00000512059.1:n.*1460+126C>T
ENST00000695620.1:c.*1676+126C>T	ENSP00000512060.1:n.*1676+126C>T
ENST00000695621.1:c.*175+126C>T	ENSP00000512061.1:n.*175+126C>T
ENST00000695622.1:c.1687+126C>T	ENSP00000512062.1:n.1687+126C>T
ENST00000695623.1:c.1744+126C>T	ENSP00000512063.1:n.1744+126C>T
ENST00000695624.1:n.1055+126C>T
ENST00000695625.1:c.1750+126C>T	ENSP00000512064.1:n.1750+126C>T
ENST00000695626.1:c.505+126C>T	ENSP00000512065.1:n.505+126C>T
ENST00000695627.1:c.698+126C>T	ENSP00000512066.1:n.698+126C>T
ENST00000695628.1:c.309+126C>T	ENSP00000512067.1:n.309+126C>T
ENST00000695629.1:c.191-393C>T	ENSP00000512068.1:n.191-393C>T
ENST00000695630.1:c.477+126C>T
ENST00000695631.1:c.115-496C>T
ENST00000703407.1:c.1222+126C>T	ENSP00000512057.1:n.1222+126C>T
ENST00000308731.8:c.1750+126C>T MANE Select	ENSP00000308176.8:n.1750+126C>T
ENST00000308731.7:c.1750+126C>T	ENSP00000308176.7:n.1750+126C>T
ENST00000372880.5:c.1222+126C>T	ENSP00000361971.1:n.1222+126C>T
ENST00000470069.1:n.115+126C>T
ENST00000488970.1:n.352+126C>T
ENST00000618050.4:c.1749+126C>T	ENSP00000479125.1:n.1749+126C>T
ENST00000621635.4:c.1852+126C>T	ENSP00000483570.1:n.1852+126C>T
NM_000061.2:c.1750+126C>T , LRG_128t1:c.1750+126C>T	NP_000052.1:n.1750+126C>T
NM_001287344.1:c.1852+126C>T	NP_001274273.1:n.1852+126C>T
NM_001287345.1:c.1222+126C>T	NP_001274274.1:n.1222+126C>T
NM_000061.3:c.1750+126C>T MANE Select	NP_000052.1:n.1750+126C>T
NM_001287344.2:c.1852+126C>T	NP_001274273.1:n.1852+126C>T
NM_001287345.2:c.1222+126C>T	NP_001274274.1:n.1222+126C>T