Canonical Allele Identifier: CA2695235453
Gene: BTK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101357574_101357586del , CM000685.2:g.101357574_101357586del GRCh38
NC_000023.10:g.100612562_100612574del , CM000685.1:g.100612562_100612574del GRCh37
NC_000023.9:g.100499218_100499230del NCBI36
NG_009616.1:g.33643_33655del , LRG_128:g.33643_33655del

Transcript Alleles

HGVS Amino-acid Change
ENST00000478995.2:n.1264_1276del
ENST00000488970.2:n.1262_1274del
ENST00000695614.1:c.1104_1116del
ENST00000695615.1:c.1104_1116del
ENST00000695616.1:c.*949_*961del
ENST00000695617.1:c.1101_1113del
ENST00000695618.1:c.*853_*865del
ENST00000695619.1:c.*814_*826del
ENST00000695620.1:c.*949_*961del
ENST00000695621.1:c.1104_1116del
ENST00000695622.1:c.1041_1053del
ENST00000695623.1:c.1098_1110del
ENST00000695624.1:n.409_421del
ENST00000695625.1:c.1104_1116del
ENST00000695626.1:c.117_129del
ENST00000695627.1:c.117_129del
ENST00000695628.1:c.117_129del
ENST00000695629.1:c.117_129del
ENST00000695630.1:c.113_125del
ENST00000695631.1:c.114+728_114+740del
ENST00000695632.1:n.121_133del
ENST00000703407.1:c.1038+792_1038+804del ENSP00000512057.1:n.1038+792_1038+804del
ENST00000308731.8:c.1104_1116del
ENST00000308731.7:c.1104_1116del
ENST00000372880.5:c.1038+792_1038+804del ENSP00000361971.1:n.1038+792_1038+804del
ENST00000470329.1:n.54_66del
ENST00000618050.4:c.1104_1116del
ENST00000621635.4:c.1206_1218del
NM_000061.2:c.1104_1116del , LRG_128t1:c.1104_1116del
NM_001287344.1:c.1206_1218del
NM_001287345.1:c.1038+792_1038+804del NP_001274274.1:n.1038+792_1038+804del
NM_000061.3:c.1104_1116del
NM_001287344.2:c.1206_1218del
NM_001287345.2:c.1038+792_1038+804del NP_001274274.1:n.1038+792_1038+804del