Canonical Allele Identifier: CA2738823436

Gene: BTK

Linked Data

• dbSNP Id: rs2147424823

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101353862C>A , CM000685.2:g.101353862C>A	GRCh38
NC_000023.10:g.100608850C>A , CM000685.1:g.100608850C>A	GRCh37
NC_000023.9:g.100495506C>A	NCBI36
NG_009616.1:g.37363G>T , LRG_128:g.37363G>T
NG_011734.1:g.108G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000478995.2:n.3267+8G>T
ENST00000488970.2:n.3906+8G>T
ENST00000695614.1:c.1750+8G>T	ENSP00000512053.1:n.1750+8G>T
ENST00000695615.1:c.1750+8G>T	ENSP00000512054.1:n.1750+8G>T
ENST00000695616.1:c.*1595+8G>T	ENSP00000512055.1:n.*1595+8G>T
ENST00000695617.1:c.1747+8G>T	ENSP00000512056.1:n.1747+8G>T
ENST00000695618.1:c.*1499+8G>T	ENSP00000512058.1:n.*1499+8G>T
ENST00000695619.1:c.*1460+8G>T	ENSP00000512059.1:n.*1460+8G>T
ENST00000695620.1:c.*1676+8G>T	ENSP00000512060.1:n.*1676+8G>T
ENST00000695621.1:c.*175+8G>T	ENSP00000512061.1:n.*175+8G>T
ENST00000695622.1:c.1687+8G>T	ENSP00000512062.1:n.1687+8G>T
ENST00000695623.1:c.1744+8G>T	ENSP00000512063.1:n.1744+8G>T
ENST00000695624.1:n.1055+8G>T
ENST00000695625.1:c.1750+8G>T	ENSP00000512064.1:n.1750+8G>T
ENST00000695626.1:c.505+8G>T	ENSP00000512065.1:n.505+8G>T
ENST00000695627.1:c.698+8G>T	ENSP00000512066.1:n.698+8G>T
ENST00000695628.1:c.309+8G>T	ENSP00000512067.1:n.309+8G>T
ENST00000695629.1:c.191-511G>T	ENSP00000512068.1:n.191-511G>T
ENST00000695630.1:c.477+8G>T
ENST00000695631.1:c.115-614G>T
ENST00000703407.1:c.1222+8G>T	ENSP00000512057.1:n.1222+8G>T
ENST00000308731.8:c.1750+8G>T MANE Select	ENSP00000308176.8:n.1750+8G>T
ENST00000308731.7:c.1750+8G>T	ENSP00000308176.7:n.1750+8G>T
ENST00000372880.5:c.1222+8G>T	ENSP00000361971.1:n.1222+8G>T
ENST00000470069.1:n.115+8G>T
ENST00000488970.1:n.352+8G>T
ENST00000618050.4:c.1749+8G>T	ENSP00000479125.1:n.1749+8G>T
ENST00000621635.4:c.1852+8G>T	ENSP00000483570.1:n.1852+8G>T
NM_000061.2:c.1750+8G>T , LRG_128t1:c.1750+8G>T	NP_000052.1:n.1750+8G>T
NM_001287344.1:c.1852+8G>T	NP_001274273.1:n.1852+8G>T
NM_001287345.1:c.1222+8G>T	NP_001274274.1:n.1222+8G>T
NM_000061.3:c.1750+8G>T MANE Select	NP_000052.1:n.1750+8G>T
NM_001287344.2:c.1852+8G>T	NP_001274273.1:n.1852+8G>T
NM_001287345.2:c.1222+8G>T	NP_001274274.1:n.1222+8G>T