Canonical Allele Identifier: CA413927877

Gene: BTK

Linked Data

• ClinVar Variation Id: 1468003
• ClinVar RCV Id: RCV001970547
• dbSNP Id: rs1057517709
• MyVariant Identifiers: chrX:g.100613336A>G (hg19) ; chrX:g.101358348A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101358348A>G , CM000685.2:g.101358348A>G	GRCh38
NC_000023.10:g.100613336A>G , CM000685.1:g.100613336A>G	GRCh37
NC_000023.9:g.100499992A>G	NCBI36
NG_009616.1:g.32877T>C , LRG_128:g.32877T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000478995.2:n.1224T>C
ENST00000488970.2:n.1222T>C
ENST00000695614.1:c.1064T>C	ENSP00000512053.1:p.Ile355Thr
ENST00000695615.1:c.1064T>C	ENSP00000512054.1:p.Ile355Thr
ENST00000695616.1:c.*909T>C	ENSP00000512055.1:n.*909T>C
ENST00000695617.1:c.1061T>C	ENSP00000512056.1:p.Ile354Thr
ENST00000695618.1:c.*813T>C	ENSP00000512058.1:n.*813T>C
ENST00000695619.1:c.*774T>C	ENSP00000512059.1:n.*774T>C
ENST00000695620.1:c.*909T>C	ENSP00000512060.1:n.*909T>C
ENST00000695621.1:c.1064T>C	ENSP00000512061.1:p.Ile355Thr
ENST00000695622.1:c.1001T>C	ENSP00000512062.1:p.Ile334Thr
ENST00000695623.1:c.1058T>C	ENSP00000512063.1:p.Ile353Thr
ENST00000695624.1:n.369T>C
ENST00000695625.1:c.1064T>C	ENSP00000512064.1:p.Ile355Thr
ENST00000695626.1:c.77T>C	ENSP00000512065.1:p.Ile26Thr
ENST00000695627.1:c.77T>C	ENSP00000512066.1:p.Ile26Thr
ENST00000695628.1:c.77T>C	ENSP00000512067.1:p.Ile26Thr
ENST00000695629.1:c.77T>C	ENSP00000512068.1:p.Ile26Thr
ENST00000695630.1:c.73T>C
ENST00000695631.1:c.76T>C
ENST00000695632.1:n.81T>C
ENST00000703407.1:c.1038+26T>C	ENSP00000512057.1:n.1038+26T>C
ENST00000308731.8:c.1064T>C MANE Select	ENSP00000308176.8:p.Ile355Thr
ENST00000308731.7:c.1064T>C	ENSP00000308176.7:p.Ile355Thr
ENST00000372880.5:c.1038+26T>C	ENSP00000361971.1:n.1038+26T>C
ENST00000470329.1:n.14T>C
ENST00000618050.4:c.1064T>C	ENSP00000479125.1:p.Ile355Thr
ENST00000621635.4:c.1166T>C	ENSP00000483570.1:p.Ile389Thr
NM_000061.2:c.1064T>C , LRG_128t1:c.1064T>C	NP_000052.1:p.Ile355Thr
NM_001287344.1:c.1166T>C	NP_001274273.1:p.Ile389Thr
NM_001287345.1:c.1038+26T>C	NP_001274274.1:n.1038+26T>C
NM_000061.3:c.1064T>C MANE Select	NP_000052.1:p.Ile355Thr
NM_001287344.2:c.1166T>C	NP_001274273.1:p.Ile389Thr
NM_001287345.2:c.1038+26T>C	NP_001274274.1:n.1038+26T>C