Canonical Allele Identifier: CA413927952
Gene: BTK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101358356G>C , CM000685.2:g.101358356G>C GRCh38
NC_000023.10:g.100613344G>C , CM000685.1:g.100613344G>C GRCh37
NC_000023.9:g.100500000G>C NCBI36
NG_009616.1:g.32869C>G , LRG_128:g.32869C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000478995.2:n.1216C>G
ENST00000488970.2:n.1214C>G
ENST00000695614.1:c.1056C>G ENSP00000512053.1:p.Phe352Leu
ENST00000695615.1:c.1056C>G ENSP00000512054.1:p.Phe352Leu
ENST00000695616.1:c.*901C>G ENSP00000512055.1:n.*901C>G
ENST00000695617.1:c.1053C>G ENSP00000512056.1:p.Phe351Leu
ENST00000695618.1:c.*805C>G ENSP00000512058.1:n.*805C>G
ENST00000695619.1:c.*766C>G ENSP00000512059.1:n.*766C>G
ENST00000695620.1:c.*901C>G ENSP00000512060.1:n.*901C>G
ENST00000695621.1:c.1056C>G ENSP00000512061.1:p.Phe352Leu
ENST00000695622.1:c.993C>G ENSP00000512062.1:p.Phe331Leu
ENST00000695623.1:c.1050C>G ENSP00000512063.1:p.Phe350Leu
ENST00000695624.1:n.361C>G
ENST00000695625.1:c.1056C>G ENSP00000512064.1:p.Phe352Leu
ENST00000695626.1:c.69C>G ENSP00000512065.1:p.Phe23Leu
ENST00000695627.1:c.69C>G ENSP00000512066.1:p.Phe23Leu
ENST00000695628.1:c.69C>G ENSP00000512067.1:p.Phe23Leu
ENST00000695629.1:c.69C>G ENSP00000512068.1:p.Phe23Leu
ENST00000695630.1:c.65C>G
ENST00000695631.1:c.68C>G
ENST00000695632.1:n.73C>G
ENST00000703407.1:c.1038+18C>G ENSP00000512057.1:n.1038+18C>G
ENST00000308731.8:c.1056C>G MANE Select ENSP00000308176.8:p.Phe352Leu
ENST00000308731.7:c.1056C>G ENSP00000308176.7:p.Phe352Leu
ENST00000372880.5:c.1038+18C>G ENSP00000361971.1:n.1038+18C>G
ENST00000470329.1:n.6C>G
ENST00000618050.4:c.1056C>G ENSP00000479125.1:p.Phe352Leu
ENST00000621635.4:c.1158C>G ENSP00000483570.1:p.Phe386Leu
NM_000061.2:c.1056C>G , LRG_128t1:c.1056C>G NP_000052.1:p.Phe352Leu
NM_001287344.1:c.1158C>G NP_001274273.1:p.Phe386Leu
NM_001287345.1:c.1038+18C>G NP_001274274.1:n.1038+18C>G
NM_000061.3:c.1056C>G MANE Select NP_000052.1:p.Phe352Leu
NM_001287344.2:c.1158C>G NP_001274273.1:p.Phe386Leu
NM_001287345.2:c.1038+18C>G NP_001274274.1:n.1038+18C>G