Canonical Allele Identifier: CA643537089

Gene: BTK

Linked Data

• ClinVar Variation Id: 2837677
• ClinVar RCV Id: RCV003625622
• dbSNP Id: rs1555977937
• gnomAD v2: X-100611951-T-A
• gnomAD v3: X-101356963-T-A
• gnomAD v4: X-101356963-T-A
• MyVariant Identifiers: chrX:g.100611951T>A (hg19) ; chrX:g.101356963T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101356963T>A , CM000685.2:g.101356963T>A	GRCh38
NC_000023.10:g.100611951T>A , CM000685.1:g.100611951T>A	GRCh37
NC_000023.9:g.100498607T>A	NCBI36
NG_009616.1:g.34262A>T , LRG_128:g.34262A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000478995.2:n.1338-8A>T
ENST00000488970.2:n.1336-8A>T
ENST00000695614.1:c.1178-8A>T	ENSP00000512053.1:n.1178-8A>T
ENST00000695615.1:c.1178-8A>T	ENSP00000512054.1:n.1178-8A>T
ENST00000695616.1:c.*1023-8A>T	ENSP00000512055.1:n.*1023-8A>T
ENST00000695617.1:c.1175-8A>T	ENSP00000512056.1:n.1175-8A>T
ENST00000695618.1:c.*927-8A>T	ENSP00000512058.1:n.*927-8A>T
ENST00000695619.1:c.*888-8A>T	ENSP00000512059.1:n.*888-8A>T
ENST00000695620.1:c.*1023-8A>T	ENSP00000512060.1:n.*1023-8A>T
ENST00000695621.1:c.1178-8A>T	ENSP00000512061.1:n.1178-8A>T
ENST00000695622.1:c.1115-8A>T	ENSP00000512062.1:n.1115-8A>T
ENST00000695623.1:c.1172-8A>T	ENSP00000512063.1:n.1172-8A>T
ENST00000695624.1:n.483-8A>T
ENST00000695625.1:c.1178-8A>T	ENSP00000512064.1:n.1178-8A>T
ENST00000695626.1:c.191-49A>T	ENSP00000512065.1:n.191-49A>T
ENST00000695627.1:c.191-8A>T	ENSP00000512066.1:n.191-8A>T
ENST00000695628.1:c.190+546A>T	ENSP00000512067.1:n.190+546A>T
ENST00000695629.1:c.190+546A>T	ENSP00000512068.1:n.190+546A>T
ENST00000695630.1:c.187-8A>T
ENST00000695631.1:c.114+1347A>T
ENST00000695632.1:n.195-8A>T
ENST00000703407.1:c.1038+1411A>T	ENSP00000512057.1:n.1038+1411A>T
ENST00000308731.8:c.1178-8A>T MANE Select	ENSP00000308176.8:n.1178-8A>T
ENST00000308731.7:c.1178-8A>T	ENSP00000308176.7:n.1178-8A>T
ENST00000372880.5:c.1038+1411A>T	ENSP00000361971.1:n.1038+1411A>T
ENST00000470329.1:n.128-8A>T
ENST00000618050.4:c.1178-8A>T	ENSP00000479125.1:n.1178-8A>T
ENST00000621635.4:c.1280-8A>T	ENSP00000483570.1:n.1280-8A>T
NM_000061.2:c.1178-8A>T , LRG_128t1:c.1178-8A>T	NP_000052.1:n.1178-8A>T
NM_001287344.1:c.1280-8A>T	NP_001274273.1:n.1280-8A>T
NM_001287345.1:c.1038+1411A>T	NP_001274274.1:n.1038+1411A>T
NM_000061.3:c.1178-8A>T MANE Select	NP_000052.1:n.1178-8A>T
NM_001287344.2:c.1280-8A>T	NP_001274273.1:n.1280-8A>T
NM_001287345.2:c.1038+1411A>T	NP_001274274.1:n.1038+1411A>T