Canonical Allele Identifier: CA413918849

Gene: BTK

Linked Data

• MyVariant Identifiers: chrX:g.100608241A>T (hg19) ; chrX:g.101353253A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101353253A>T , CM000685.2:g.101353253A>T	GRCh38
NC_000023.10:g.100608241A>T , CM000685.1:g.100608241A>T	GRCh37
NC_000023.9:g.100494897A>T	NCBI36
NG_009616.1:g.37972T>A , LRG_128:g.37972T>A
NG_011734.1:g.717T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478995.2:n.3366T>A
ENST00000488970.2:n.4005T>A
ENST00000695614.1:c.1849T>A	ENSP00000512053.1:p.Tyr617Asn
ENST00000695615.1:c.1849T>A	ENSP00000512054.1:p.Tyr617Asn
ENST00000695616.1:c.*1694T>A	ENSP00000512055.1:n.*1694T>A
ENST00000695617.1:c.1846T>A	ENSP00000512056.1:p.Tyr616Asn
ENST00000695618.1:c.*1598T>A	ENSP00000512058.1:n.*1598T>A
ENST00000695619.1:c.*1559T>A	ENSP00000512059.1:n.*1559T>A
ENST00000695620.1:c.*1775T>A	ENSP00000512060.1:n.*1775T>A
ENST00000695621.1:c.*274T>A	ENSP00000512061.1:n.*274T>A
ENST00000695622.1:c.1786T>A	ENSP00000512062.1:p.Tyr596Asn
ENST00000695623.1:c.1843T>A	ENSP00000512063.1:p.Tyr615Asn
ENST00000695624.1:n.1154T>A
ENST00000695625.1:c.1849T>A	ENSP00000512064.1:p.Tyr617Asn
ENST00000695626.1:c.604T>A	ENSP00000512065.1:n.604T>A
ENST00000695627.1:c.797T>A	ENSP00000512066.1:n.797T>A
ENST00000695628.1:c.408T>A	ENSP00000512067.1:n.408T>A
ENST00000695629.1:c.289T>A	ENSP00000512068.1:p.Tyr97Asn
ENST00000695630.1:c.576T>A
ENST00000695631.1:c.115-5T>A
ENST00000703407.1:c.1321T>A	ENSP00000512057.1:p.Tyr441Asn
ENST00000308731.8:c.1849T>A MANE Select	ENSP00000308176.8:p.Tyr617Asn
ENST00000308731.7:c.1849T>A	ENSP00000308176.7:p.Tyr617Asn
ENST00000372880.5:c.1321T>A	ENSP00000361971.1:p.Tyr441Asn
ENST00000470069.1:n.214T>A
ENST00000618050.4:c.1848T>A	ENSP00000479125.1:n.1848T>A
ENST00000621635.4:c.1951T>A	ENSP00000483570.1:p.Tyr651Asn
NM_000061.2:c.1849T>A , LRG_128t1:c.1849T>A	NP_000052.1:p.Tyr617Asn
NM_001287344.1:c.1951T>A	NP_001274273.1:p.Tyr651Asn
NM_001287345.1:c.1321T>A	NP_001274274.1:p.Tyr441Asn
NM_000061.3:c.1849T>A MANE Select	NP_000052.1:p.Tyr617Asn
NM_001287344.2:c.1951T>A	NP_001274273.1:p.Tyr651Asn
NM_001287345.2:c.1321T>A	NP_001274274.1:p.Tyr441Asn