Canonical Allele Identifier: CA916081271

Gene: BTK

Linked Data

• ClinVar Variation Id: 836009
• ClinVar RCV Id: RCV001037029

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101350769_101356833del , CM000685.2:g.101350769_101356833del	GRCh38
NC_000023.10:g.100605757_100611821del , CM000685.1:g.100605757_100611821del	GRCh37
NC_000023.9:g.100492413_100498477del	NCBI36
NG_009616.1:g.34392_40456del , LRG_128:g.34392_40456del

Transcript Alleles

HGVS	Amino-acid change
ENST00000478995.2:n.1460_3426-813del
ENST00000488970.2:n.1458_4065-813del
ENST00000695614.1:c.1300_1909-813del
ENST00000695615.1:c.1300_1909-813del
ENST00000695616.1:c.*1145_*1754-813del
ENST00000695617.1:c.1297_1906-813del
ENST00000695618.1:c.*1049_*1658-813del
ENST00000695619.1:c.*1010_*1619-813del
ENST00000695620.1:c.*1145_*1835-813del
ENST00000695621.1:c.1300_*334-813del
ENST00000695622.1:c.1237_1846-813del
ENST00000695623.1:c.1294_1903-813del
ENST00000695624.1:n.605_1214-813del
ENST00000695625.1:c.1300_1876-813del
ENST00000695626.1:c.272_664-813del
ENST00000695627.1:c.313_857-813del
ENST00000695628.1:c.190+676_468-813del
ENST00000695629.1:c.190+676_349-813del
ENST00000695630.1:c.309_636-813del
ENST00000695631.1:c.114+1477_170-813del
ENST00000703407.1:c.1038+1541_1381-813del
ENST00000308731.8:c.1300_1909-813del
ENST00000308731.7:c.1300_1909-813del
ENST00000372880.5:c.1038+1541_1381-813del
ENST00000618050.4:c.1300_1908-813del
ENST00000621635.4:c.1402_2011-813del
NM_000061.2:c.1300_1909-813del , LRG_128t1:c.1300_1909-813del
NM_001287344.1:c.1402_2011-813del
NM_001287345.1:c.1038+1541_1381-813del
NM_000061.3:c.1300_1909-813del
NM_001287344.2:c.1402_2011-813del
NM_001287345.2:c.1038+1541_1381-813del