Canonical Allele Identifier: CA413929684
Gene: BTK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101359299C>G , CM000685.2:g.101359299C>G GRCh38
NC_000023.10:g.100614287C>G , CM000685.1:g.100614287C>G GRCh37
NC_000023.9:g.100500943C>G NCBI36
NG_009616.1:g.31926G>C , LRG_128:g.31926G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000464006.2:n.668G>C
ENST00000478995.2:n.1048G>C
ENST00000488970.2:n.1046G>C
ENST00000695614.1:c.888G>C ENSP00000512053.1:p.Lys296Asn
ENST00000695615.1:c.888G>C ENSP00000512054.1:p.Lys296Asn
ENST00000695616.1:c.*733G>C ENSP00000512055.1:n.*733G>C
ENST00000695617.1:c.885G>C ENSP00000512056.1:p.Lys295Asn
ENST00000695618.1:c.*637G>C ENSP00000512058.1:n.*637G>C
ENST00000695619.1:c.*684+789G>C ENSP00000512059.1:n.*684+789G>C
ENST00000695620.1:c.*733G>C ENSP00000512060.1:n.*733G>C
ENST00000695621.1:c.888G>C ENSP00000512061.1:p.Lys296Asn
ENST00000695622.1:c.825G>C ENSP00000512062.1:p.Lys275Asn
ENST00000695623.1:c.882G>C ENSP00000512063.1:p.Lys294Asn
ENST00000695624.1:n.193G>C
ENST00000695625.1:c.888G>C ENSP00000512064.1:p.Lys296Asn
ENST00000703407.1:c.888G>C ENSP00000512057.1:p.Lys296Asn
ENST00000308731.8:c.888G>C MANE Select ENSP00000308176.8:p.Lys296Asn
ENST00000308731.7:c.888G>C ENSP00000308176.7:p.Lys296Asn
ENST00000372880.5:c.888G>C ENSP00000361971.1:p.Lys296Asn
ENST00000618050.4:c.888G>C ENSP00000479125.1:p.Lys296Asn
ENST00000621635.4:c.990G>C ENSP00000483570.1:p.Lys330Asn
NM_000061.2:c.888G>C , LRG_128t1:c.888G>C NP_000052.1:p.Lys296Asn
NM_001287344.1:c.990G>C NP_001274273.1:p.Lys330Asn
NM_001287345.1:c.888G>C NP_001274274.1:p.Lys296Asn
NM_000061.3:c.888G>C MANE Select NP_000052.1:p.Lys296Asn
NM_001287344.2:c.990G>C NP_001274273.1:p.Lys330Asn
NM_001287345.2:c.888G>C NP_001274274.1:p.Lys296Asn