Canonical Allele Identifier: CA413927906
Gene: BTK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101358352T>G , CM000685.2:g.101358352T>G GRCh38
NC_000023.10:g.100613340T>G , CM000685.1:g.100613340T>G GRCh37
NC_000023.9:g.100499996T>G NCBI36
NG_009616.1:g.32873A>C , LRG_128:g.32873A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000478995.2:n.1220A>C
ENST00000488970.2:n.1218A>C
ENST00000695614.1:c.1060A>C ENSP00000512053.1:p.Thr354Pro
ENST00000695615.1:c.1060A>C ENSP00000512054.1:p.Thr354Pro
ENST00000695616.1:c.*905A>C ENSP00000512055.1:n.*905A>C
ENST00000695617.1:c.1057A>C ENSP00000512056.1:p.Thr353Pro
ENST00000695618.1:c.*809A>C ENSP00000512058.1:n.*809A>C
ENST00000695619.1:c.*770A>C ENSP00000512059.1:n.*770A>C
ENST00000695620.1:c.*905A>C ENSP00000512060.1:n.*905A>C
ENST00000695621.1:c.1060A>C ENSP00000512061.1:p.Thr354Pro
ENST00000695622.1:c.997A>C ENSP00000512062.1:p.Thr333Pro
ENST00000695623.1:c.1054A>C ENSP00000512063.1:p.Thr352Pro
ENST00000695624.1:n.365A>C
ENST00000695625.1:c.1060A>C ENSP00000512064.1:p.Thr354Pro
ENST00000695626.1:c.73A>C ENSP00000512065.1:p.Thr25Pro
ENST00000695627.1:c.73A>C ENSP00000512066.1:p.Thr25Pro
ENST00000695628.1:c.73A>C ENSP00000512067.1:p.Thr25Pro
ENST00000695629.1:c.73A>C ENSP00000512068.1:p.Thr25Pro
ENST00000695630.1:c.69A>C
ENST00000695631.1:c.72A>C
ENST00000695632.1:n.77A>C
ENST00000703407.1:c.1038+22A>C ENSP00000512057.1:n.1038+22A>C
ENST00000308731.8:c.1060A>C MANE Select ENSP00000308176.8:p.Thr354Pro
ENST00000308731.7:c.1060A>C ENSP00000308176.7:p.Thr354Pro
ENST00000372880.5:c.1038+22A>C ENSP00000361971.1:n.1038+22A>C
ENST00000470329.1:n.10A>C
ENST00000618050.4:c.1060A>C ENSP00000479125.1:p.Thr354Pro
ENST00000621635.4:c.1162A>C ENSP00000483570.1:p.Thr388Pro
NM_000061.2:c.1060A>C , LRG_128t1:c.1060A>C NP_000052.1:p.Thr354Pro
NM_001287344.1:c.1162A>C NP_001274273.1:p.Thr388Pro
NM_001287345.1:c.1038+22A>C NP_001274274.1:n.1038+22A>C
NM_000061.3:c.1060A>C MANE Select NP_000052.1:p.Thr354Pro
NM_001287344.2:c.1162A>C NP_001274273.1:p.Thr388Pro
NM_001287345.2:c.1038+22A>C NP_001274274.1:n.1038+22A>C