Canonical Allele Identifier: CA2694291766

Gene: BTK

Linked Data

• gnomAD v4: X-101357367-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101357371dup , CM000685.2:g.101357371dup	GRCh38
NC_000023.10:g.100612359dup , CM000685.1:g.100612359dup	GRCh37
NC_000023.9:g.100499015dup	NCBI36
NG_009616.1:g.33857dup , LRG_128:g.33857dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478995.2:n.1337+141dup
ENST00000488970.2:n.1335+141dup
ENST00000695614.1:c.1177+141dup	ENSP00000512053.1:n.1177+141dup
ENST00000695615.1:c.1177+141dup	ENSP00000512054.1:n.1177+141dup
ENST00000695616.1:c.*1022+141dup	ENSP00000512055.1:n.*1022+141dup
ENST00000695617.1:c.1174+141dup	ENSP00000512056.1:n.1174+141dup
ENST00000695618.1:c.*926+141dup	ENSP00000512058.1:n.*926+141dup
ENST00000695619.1:c.*887+141dup	ENSP00000512059.1:n.*887+141dup
ENST00000695620.1:c.*1022+141dup	ENSP00000512060.1:n.*1022+141dup
ENST00000695621.1:c.1177+141dup	ENSP00000512061.1:n.1177+141dup
ENST00000695622.1:c.1114+141dup	ENSP00000512062.1:n.1114+141dup
ENST00000695623.1:c.1171+141dup	ENSP00000512063.1:n.1171+141dup
ENST00000695624.1:n.482+141dup
ENST00000695625.1:c.1177+141dup	ENSP00000512064.1:n.1177+141dup
ENST00000695626.1:c.190+141dup	ENSP00000512065.1:n.190+141dup
ENST00000695627.1:c.190+141dup	ENSP00000512066.1:n.190+141dup
ENST00000695628.1:c.190+141dup	ENSP00000512067.1:n.190+141dup
ENST00000695629.1:c.190+141dup	ENSP00000512068.1:n.190+141dup
ENST00000695630.1:c.186+141dup
ENST00000695631.1:c.114+942dup
ENST00000695632.1:n.194+141dup
ENST00000703407.1:c.1038+1006dup	ENSP00000512057.1:n.1038+1006dup
ENST00000308731.8:c.1177+141dup MANE Select	ENSP00000308176.8:n.1177+141dup
ENST00000308731.7:c.1177+141dup	ENSP00000308176.7:n.1177+141dup
ENST00000372880.5:c.1038+1006dup	ENSP00000361971.1:n.1038+1006dup
ENST00000470329.1:n.127+141dup
ENST00000618050.4:c.1177+141dup	ENSP00000479125.1:n.1177+141dup
ENST00000621635.4:c.1279+141dup	ENSP00000483570.1:n.1279+141dup
NM_000061.2:c.1177+141dup , LRG_128t1:c.1177+141dup	NP_000052.1:n.1177+141dup
NM_001287344.1:c.1279+141dup	NP_001274273.1:n.1279+141dup
NM_001287345.1:c.1038+1006dup	NP_001274274.1:n.1038+1006dup
NM_000061.3:c.1177+141dup MANE Select	NP_000052.1:n.1177+141dup
NM_001287344.2:c.1279+141dup	NP_001274273.1:n.1279+141dup
NM_001287345.2:c.1038+1006dup	NP_001274274.1:n.1038+1006dup