Canonical Allele Identifier: CA2448284060
Gene: BTK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101357486_101357487delinsAC , CM000685.2:g.101357486_101357487delinsAC GRCh38
NC_000023.10:g.100612474_100612475delinsAC , CM000685.1:g.100612474_100612475delinsAC GRCh37
NC_000023.9:g.100499130_100499131delinsAC NCBI36
NG_009616.1:g.33738_33739delinsGT , LRG_128:g.33738_33739delinsGT

Transcript Alleles

HGVS Amino-acid change
ENST00000478995.2:n.1337+22_1337+23delinsGT
ENST00000488970.2:n.1335+22_1335+23delinsGT
ENST00000695614.1:c.1177+22_1177+23delinsGT ENSP00000512053.1:n.1177+22_1177+23delins...
ENST00000695615.1:c.1177+22_1177+23delinsGT ENSP00000512054.1:n.1177+22_1177+23delins...
ENST00000695616.1:c.*1022+22_*1022+23delinsGT ENSP00000512055.1:n.*1022+22_*1022+23deli...
ENST00000695617.1:c.1174+22_1174+23delinsGT ENSP00000512056.1:n.1174+22_1174+23delins...
ENST00000695618.1:c.*926+22_*926+23delinsGT ENSP00000512058.1:n.*926+22_*926+23delins...
ENST00000695619.1:c.*887+22_*887+23delinsGT ENSP00000512059.1:n.*887+22_*887+23delins...
ENST00000695620.1:c.*1022+22_*1022+23delinsGT ENSP00000512060.1:n.*1022+22_*1022+23deli...
ENST00000695621.1:c.1177+22_1177+23delinsGT ENSP00000512061.1:n.1177+22_1177+23delins...
ENST00000695622.1:c.1114+22_1114+23delinsGT ENSP00000512062.1:n.1114+22_1114+23delins...
ENST00000695623.1:c.1171+22_1171+23delinsGT ENSP00000512063.1:n.1171+22_1171+23delins...
ENST00000695624.1:n.482+22_482+23delinsGT
ENST00000695625.1:c.1177+22_1177+23delinsGT ENSP00000512064.1:n.1177+22_1177+23delins...
ENST00000695626.1:c.190+22_190+23delinsGT ENSP00000512065.1:n.190+22_190+23delinsGT...
ENST00000695627.1:c.190+22_190+23delinsGT ENSP00000512066.1:n.190+22_190+23delinsGT...
ENST00000695628.1:c.190+22_190+23delinsGT ENSP00000512067.1:n.190+22_190+23delinsGT...
ENST00000695629.1:c.190+22_190+23delinsGT ENSP00000512068.1:n.190+22_190+23delinsGT...
ENST00000695630.1:c.186+22_186+23delinsGT
ENST00000695631.1:c.114+823_114+824delinsGT
ENST00000695632.1:n.194+22_194+23delinsGT
ENST00000703407.1:c.1038+887_1038+888delinsGT ENSP00000512057.1:n.1038+887_1038+888deli...
ENST00000308731.8:c.1177+22_1177+23delinsGT MANE Select ENSP00000308176.8:n.1177+22_1177+23delins...
ENST00000308731.7:c.1177+22_1177+23delinsGT ENSP00000308176.7:n.1177+22_1177+23delins...
ENST00000372880.5:c.1038+887_1038+888delinsGT ENSP00000361971.1:n.1038+887_1038+888deli...
ENST00000470329.1:n.127+22_127+23delinsGT
ENST00000618050.4:c.1177+22_1177+23delinsGT ENSP00000479125.1:n.1177+22_1177+23delins...
ENST00000621635.4:c.1279+22_1279+23delinsGT ENSP00000483570.1:n.1279+22_1279+23delins...
NM_000061.2:c.1177+22_1177+23delinsGT , LRG_128t1:c.1177+22_1177+23delinsGT NP_000052.1:n.1177+22_1177+23delinsGT
NM_001287344.1:c.1279+22_1279+23delinsGT NP_001274273.1:n.1279+22_1279+23delinsGT
NM_001287345.1:c.1038+887_1038+888delinsGT NP_001274274.1:n.1038+887_1038+888delinsG...
NM_000061.3:c.1177+22_1177+23delinsGT MANE Select NP_000052.1:n.1177+22_1177+23delinsGT
NM_001287344.2:c.1279+22_1279+23delinsGT NP_001274273.1:n.1279+22_1279+23delinsGT
NM_001287345.2:c.1038+887_1038+888delinsGT NP_001274274.1:n.1038+887_1038+888delinsG...