Canonical Allele Identifier: CA2694292064

Gene: BTK

Linked Data

• gnomAD v4: X-101357661-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101357661A>G , CM000685.2:g.101357661A>G	GRCh38
NC_000023.10:g.100612649A>G , CM000685.1:g.100612649A>G	GRCh37
NC_000023.9:g.100499305A>G	NCBI36
NG_009616.1:g.33564T>C , LRG_128:g.33564T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478995.2:n.1263-78T>C
ENST00000488970.2:n.1261-78T>C
ENST00000695614.1:c.1103-78T>C	ENSP00000512053.1:n.1103-78T>C
ENST00000695615.1:c.1103-78T>C	ENSP00000512054.1:n.1103-78T>C
ENST00000695616.1:c.*948-78T>C	ENSP00000512055.1:n.*948-78T>C
ENST00000695617.1:c.1100-78T>C	ENSP00000512056.1:n.1100-78T>C
ENST00000695618.1:c.*852-78T>C	ENSP00000512058.1:n.*852-78T>C
ENST00000695619.1:c.*813-78T>C	ENSP00000512059.1:n.*813-78T>C
ENST00000695620.1:c.*948-78T>C	ENSP00000512060.1:n.*948-78T>C
ENST00000695621.1:c.1103-78T>C	ENSP00000512061.1:n.1103-78T>C
ENST00000695622.1:c.1040-78T>C	ENSP00000512062.1:n.1040-78T>C
ENST00000695623.1:c.1097-78T>C	ENSP00000512063.1:n.1097-78T>C
ENST00000695624.1:n.408-78T>C
ENST00000695625.1:c.1103-78T>C	ENSP00000512064.1:n.1103-78T>C
ENST00000695626.1:c.116-78T>C	ENSP00000512065.1:n.116-78T>C
ENST00000695627.1:c.116-78T>C	ENSP00000512066.1:n.116-78T>C
ENST00000695628.1:c.116-78T>C	ENSP00000512067.1:n.116-78T>C
ENST00000695629.1:c.116-78T>C	ENSP00000512068.1:n.116-78T>C
ENST00000695630.1:c.112-78T>C
ENST00000695631.1:c.114+649T>C
ENST00000695632.1:n.120-78T>C
ENST00000703407.1:c.1038+713T>C	ENSP00000512057.1:n.1038+713T>C
ENST00000308731.8:c.1103-78T>C MANE Select	ENSP00000308176.8:n.1103-78T>C
ENST00000308731.7:c.1103-78T>C	ENSP00000308176.7:n.1103-78T>C
ENST00000372880.5:c.1038+713T>C	ENSP00000361971.1:n.1038+713T>C
ENST00000470329.1:n.53-78T>C
ENST00000618050.4:c.1103-78T>C	ENSP00000479125.1:n.1103-78T>C
ENST00000621635.4:c.1205-78T>C	ENSP00000483570.1:n.1205-78T>C
NM_000061.2:c.1103-78T>C , LRG_128t1:c.1103-78T>C	NP_000052.1:n.1103-78T>C
NM_001287344.1:c.1205-78T>C	NP_001274273.1:n.1205-78T>C
NM_001287345.1:c.1038+713T>C	NP_001274274.1:n.1038+713T>C
NM_000061.3:c.1103-78T>C MANE Select	NP_000052.1:n.1103-78T>C
NM_001287344.2:c.1205-78T>C	NP_001274273.1:n.1205-78T>C
NM_001287345.2:c.1038+713T>C	NP_001274274.1:n.1038+713T>C