Canonical Allele Identifier: CA2695235456

Gene: BTK

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101358313_101358440del , CM000685.2:g.101358313_101358440del	GRCh38
NC_000023.10:g.100613301_100613428del , CM000685.1:g.100613301_100613428del	GRCh37
NC_000023.9:g.100499957_100500084del	NCBI36
NG_009616.1:g.32789_32916del , LRG_128:g.32789_32916del

Transcript Alleles

HGVS	Amino-acid change
ENST00000478995.2:n.1136_1262+1del
ENST00000488970.2:n.1134_1260+1del
ENST00000695614.1:c.976_1102+1del
ENST00000695615.1:c.976_1102+1del
ENST00000695616.1:c.*821_*947+1del
ENST00000695617.1:c.973_1099+1del
ENST00000695618.1:c.*725_*851+1del
ENST00000695619.1:c.*686_*812+1del
ENST00000695620.1:c.*821_*947+1del
ENST00000695621.1:c.976_1102+1del
ENST00000695622.1:c.913_1039+1del
ENST00000695623.1:c.970_1096+1del
ENST00000695624.1:n.281_407+1del
ENST00000695625.1:c.976_1102+1del
ENST00000703407.1:c.976_1038+65del
ENST00000308731.8:c.976_1102+1del
ENST00000308731.7:c.976_1102+1del
ENST00000372880.5:c.976_1038+65del
ENST00000618050.4:c.976_1102+1del
ENST00000621635.4:c.1078_1204+1del
NM_000061.2:c.976_1102+1del , LRG_128t1:c.976_1102+1del
NM_001287344.1:c.1078_1204+1del
NM_001287345.1:c.976_1038+65del
NM_000061.3:c.976_1102+1del
NM_001287344.2:c.1078_1204+1del
NM_001287345.2:c.976_1038+65del