Canonical Allele Identifier: CA2822688511

Gene: BTK

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101353428_101353429insCAAACACACCCAAC , CM000685.2:g.101353428_101353429insCAAACACACCCAAC	GRCh38
NC_000023.10:g.100608416_100608417insCAAACACACCCAAC , CM000685.1:g.100608416_100608417insCAAACACACCCAAC	GRCh37
NC_000023.9:g.100495072_100495073insCAAACACACCCAAC	NCBI36
NG_009616.1:g.37797_37798insTTGGGTGTGTTTGG , LRG_128:g.37797_37798insTTGGGTGTGTTTGG
NG_011734.1:g.542_543insTTGGGTGTGTTTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478995.2:n.3268-77_3268-76insTTGGGTGTGTTTGG
ENST00000488970.2:n.3907-77_3907-76insTTGGGTGTGTTTGG
ENST00000695614.1:c.1751-77_1751-76insTTGGGTGTGTTTGG	ENSP00000512053.1:n.1751-77_1751-76insTTGGGTGTGTTTGG
ENST00000695615.1:c.1751-77_1751-76insTTGGGTGTGTTTGG	ENSP00000512054.1:n.1751-77_1751-76insTTGGGTGTGTTTGG
ENST00000695616.1:c.*1596-77_*1596-76insTTGGGTGTGTTTGG	ENSP00000512055.1:n.*1596-77_*1596-76insTTGGGTGTGTTTGG
ENST00000695617.1:c.1748-77_1748-76insTTGGGTGTGTTTGG	ENSP00000512056.1:n.1748-77_1748-76insTTGGGTGTGTTTGG
ENST00000695618.1:c.*1500-77_*1500-76insTTGGGTGTGTTTGG	ENSP00000512058.1:n.*1500-77_*1500-76insTTGGGTGTGTTTGG
ENST00000695619.1:c.*1461-77_*1461-76insTTGGGTGTGTTTGG	ENSP00000512059.1:n.*1461-77_*1461-76insTTGGGTGTGTTTGG
ENST00000695620.1:c.*1677-77_*1677-76insTTGGGTGTGTTTGG	ENSP00000512060.1:n.*1677-77_*1677-76insTTGGGTGTGTTTGG
ENST00000695621.1:c.*176-77_*176-76insTTGGGTGTGTTTGG	ENSP00000512061.1:n.*176-77_*176-76insTTGGGTGTGTTTGG
ENST00000695622.1:c.1688-77_1688-76insTTGGGTGTGTTTGG	ENSP00000512062.1:n.1688-77_1688-76insTTGGGTGTGTTTGG
ENST00000695623.1:c.1745-77_1745-76insTTGGGTGTGTTTGG	ENSP00000512063.1:n.1745-77_1745-76insTTGGGTGTGTTTGG
ENST00000695624.1:n.1056-77_1056-76insTTGGGTGTGTTTGG
ENST00000695625.1:c.1751-77_1751-76insTTGGGTGTGTTTGG	ENSP00000512064.1:n.1751-77_1751-76insTTGGGTGTGTTTGG
ENST00000695626.1:c.506-77_506-76insTTGGGTGTGTTTGG	ENSP00000512065.1:n.506-77_506-76insTTGGGTGTGTTTGG
ENST00000695627.1:c.699-77_699-76insTTGGGTGTGTTTGG	ENSP00000512066.1:n.699-77_699-76insTTGGGTGTGTTTGG
ENST00000695628.1:c.310-77_310-76insTTGGGTGTGTTTGG	ENSP00000512067.1:n.310-77_310-76insTTGGGTGTGTTTGG
ENST00000695629.1:c.191-77_191-76insTTGGGTGTGTTTGG	ENSP00000512068.1:n.191-77_191-76insTTGGGTGTGTTTGG
ENST00000695630.1:c.478-77_478-76insTTGGGTGTGTTTGG
ENST00000695631.1:c.115-180_115-179insTTGGGTGTGTTTGG
ENST00000703407.1:c.1223-77_1223-76insTTGGGTGTGTTTGG	ENSP00000512057.1:n.1223-77_1223-76insTTGGGTGTGTTTGG
ENST00000308731.8:c.1751-77_1751-76insTTGGGTGTGTTTGG MANE Select	ENSP00000308176.8:n.1751-77_1751-76insTTGGGTGTGTTTGG
ENST00000308731.7:c.1751-77_1751-76insTTGGGTGTGTTTGG	ENSP00000308176.7:n.1751-77_1751-76insTTGGGTGTGTTTGG
ENST00000372880.5:c.1223-77_1223-76insTTGGGTGTGTTTGG	ENSP00000361971.1:n.1223-77_1223-76insTTGGGTGTGTTTGG
ENST00000470069.1:n.116-77_116-76insTTGGGTGTGTTTGG
ENST00000488970.1:n.353-77_353-76insTTGGGTGTGTTTGG
ENST00000618050.4:c.1750-77_1750-76insTTGGGTGTGTTTGG	ENSP00000479125.1:n.1750-77_1750-76insTTGGGTGTGTTTGG
ENST00000621635.4:c.1853-77_1853-76insTTGGGTGTGTTTGG	ENSP00000483570.1:n.1853-77_1853-76insTTGGGTGTGTTTGG
NM_000061.2:c.1751-77_1751-76insTTGGGTGTGTTTGG , LRG_128t1:c.1751-77_1751-76insTTGGGTGTGTTTGG	NP_000052.1:n.1751-77_1751-76insTTGGGTGTGTTTGG
NM_001287344.1:c.1853-77_1853-76insTTGGGTGTGTTTGG	NP_001274273.1:n.1853-77_1853-76insTTGGGTGTGTTTGG
NM_001287345.1:c.1223-77_1223-76insTTGGGTGTGTTTGG	NP_001274274.1:n.1223-77_1223-76insTTGGGTGTGTTTGG
NM_000061.3:c.1751-77_1751-76insTTGGGTGTGTTTGG MANE Select	NP_000052.1:n.1751-77_1751-76insTTGGGTGTGTTTGG
NM_001287344.2:c.1853-77_1853-76insTTGGGTGTGTTTGG	NP_001274273.1:n.1853-77_1853-76insTTGGGTGTGTTTGG
NM_001287345.2:c.1223-77_1223-76insTTGGGTGTGTTTGG	NP_001274274.1:n.1223-77_1223-76insTTGGGTGTGTTTGG