Canonical Allele Identifier: CA2695235364

Gene: BTK

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101353870del , CM000685.2:g.101353870del	GRCh38
NC_000023.10:g.100608858del , CM000685.1:g.100608858del	GRCh37
NC_000023.9:g.100495514del	NCBI36
NG_009616.1:g.37356del , LRG_128:g.37356del
NG_011734.1:g.101del

Transcript Alleles

HGVS	Amino-acid change
ENST00000478995.2:n.3267+1del
ENST00000488970.2:n.3906+1del
ENST00000695614.1:c.1750+1del
ENST00000695615.1:c.1750+1del
ENST00000695616.1:c.*1595+1del
ENST00000695617.1:c.1747+1del
ENST00000695618.1:c.*1499+1del
ENST00000695619.1:c.*1460+1del
ENST00000695620.1:c.*1676+1del
ENST00000695621.1:c.*175+1del
ENST00000695622.1:c.1687+1del
ENST00000695623.1:c.1744+1del
ENST00000695624.1:n.1055+1del
ENST00000695625.1:c.1750+1del
ENST00000695626.1:c.505+1del
ENST00000695627.1:c.698+1del
ENST00000695628.1:c.309+1del
ENST00000695629.1:c.191-518del	ENSP00000512068.1:n.191-518del
ENST00000695630.1:c.477+1del
ENST00000695631.1:c.115-621del
ENST00000703407.1:c.1222+1del
ENST00000308731.8:c.1750+1del
ENST00000308731.7:c.1750+1del
ENST00000372880.5:c.1222+1del
ENST00000470069.1:n.115+1del
ENST00000488970.1:n.352+1del
ENST00000618050.4:c.1749+1del
ENST00000621635.4:c.1852+1del
NM_000061.2:c.1750+1del , LRG_128t1:c.1750+1del
NM_001287344.1:c.1852+1del
NM_001287345.1:c.1222+1del
NM_000061.3:c.1750+1del
NM_001287344.2:c.1852+1del
NM_001287345.2:c.1222+1del