Canonical Allele Identifier: CA255796

Gene: BTK

Linked Data

• ClinVar Variation Id: 11349
• ClinVar RCV Id: RCV000012102 ; RCV003511976
• dbSNP Id: rs128620186
• MyVariant Identifiers: chrX:g.100630271A>G (hg19) ; chrX:g.101375283A>G (hg38)
• PubMed: PMID:8644706

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101375283A>G , CM000685.2:g.101375283A>G	GRCh38
NC_000023.10:g.100630271A>G , CM000685.1:g.100630271A>G	GRCh37
NC_000023.9:g.100516927A>G	NCBI36
NG_009616.1:g.15942T>C , LRG_128:g.15942T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478995.2:n.162T>C
ENST00000488970.2:n.162T>C
ENST00000695614.1:c.2T>C	ENSP00000512053.1:p.Met1Thr
ENST00000695615.1:c.2T>C	ENSP00000512054.1:p.Met1Thr
ENST00000695616.1:c.2T>C	ENSP00000512055.1:p.Met1Thr
ENST00000695617.1:c.2T>C	ENSP00000512056.1:p.Met1Thr
ENST00000695618.1:c.2T>C	ENSP00000512058.1:p.Met1Thr
ENST00000695619.1:c.2T>C	ENSP00000512059.1:p.Met1Thr
ENST00000695620.1:c.2T>C	ENSP00000512060.1:p.Met1Thr
ENST00000695621.1:c.2T>C	ENSP00000512061.1:p.Met1Thr
ENST00000695622.1:c.2T>C	ENSP00000512062.1:p.Met1Thr
ENST00000695623.1:c.2T>C	ENSP00000512063.1:p.Met1Thr
ENST00000695625.1:c.2T>C	ENSP00000512064.1:p.Met1Thr
ENST00000695633.1:n.315T>C
ENST00000695643.1:c.2T>C	ENSP00000512078.1:p.Met1Thr
ENST00000703407.1:c.2T>C	ENSP00000512057.1:p.Met1Thr
ENST00000308731.8:c.2T>C MANE Select	ENSP00000308176.8:p.Met1Thr
ENST00000308731.7:c.2T>C	ENSP00000308176.7:p.Met1Thr
ENST00000372880.5:c.2T>C	ENSP00000361971.1:p.Met1Thr
ENST00000464567.1:n.119T>C
ENST00000618050.4:c.2T>C	ENSP00000479125.1:p.Met1Thr
ENST00000621635.4:c.104T>C	ENSP00000483570.1:p.Met35Thr
NM_000061.2:c.2T>C , LRG_128t1:c.2T>C	NP_000052.1:p.Met1Thr
NM_001287344.1:c.104T>C	NP_001274273.1:p.Met35Thr
NM_001287345.1:c.2T>C	NP_001274274.1:p.Met1Thr
NM_000061.3:c.2T>C MANE Select	NP_000052.1:p.Met1Thr
NM_001287344.2:c.104T>C	NP_001274273.1:p.Met35Thr
NM_001287345.2:c.2T>C	NP_001274274.1:p.Met1Thr