Canonical Allele Identifier: CA517531929

Gene: BTK

Linked Data

• gnomAD v4: X-101356061-G-A
• MyVariant Identifiers: chrX:g.100611049G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101356061G>A , CM000685.2:g.101356061G>A	GRCh38
NC_000023.10:g.100611049G>A , CM000685.1:g.100611049G>A	GRCh37
NC_000023.9:g.100497705G>A	NCBI36
NG_009616.1:g.35164C>T , LRG_128:g.35164C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000478995.2:n.1717C>T
ENST00000488970.2:n.1715C>T
ENST00000695614.1:c.1557C>T	ENSP00000512053.1:p.His519=
ENST00000695615.1:c.1557C>T	ENSP00000512054.1:p.His519=
ENST00000695616.1:c.*1402C>T	ENSP00000512055.1:n.*1402C>T
ENST00000695617.1:c.1554C>T	ENSP00000512056.1:p.His518=
ENST00000695618.1:c.*1306C>T	ENSP00000512058.1:n.*1306C>T
ENST00000695619.1:c.*1267C>T	ENSP00000512059.1:n.*1267C>T
ENST00000695620.1:c.*1483C>T	ENSP00000512060.1:n.*1483C>T
ENST00000695621.1:c.1557C>T	ENSP00000512061.1:p.His519=
ENST00000695622.1:c.1494C>T	ENSP00000512062.1:p.His498=
ENST00000695623.1:c.1551C>T	ENSP00000512063.1:p.His517=
ENST00000695624.1:n.862C>T
ENST00000695625.1:c.1557C>T	ENSP00000512064.1:p.His519=
ENST00000695626.1:c.321+723C>T	ENSP00000512065.1:n.321+723C>T
ENST00000695627.1:c.570C>T	ENSP00000512066.1:p.His190=
ENST00000695628.1:c.190+1448C>T	ENSP00000512067.1:n.190+1448C>T
ENST00000695629.1:c.190+1448C>T	ENSP00000512068.1:n.190+1448C>T
ENST00000695630.1:c.358+723C>T
ENST00000695631.1:c.114+2249C>T
ENST00000695632.1:n.366+723C>T
ENST00000703407.1:c.1039-1367C>T	ENSP00000512057.1:n.1039-1367C>T
ENST00000308731.8:c.1557C>T MANE Select	ENSP00000308176.8:p.His519=
ENST00000308731.7:c.1557C>T	ENSP00000308176.7:p.His519=
ENST00000372880.5:c.1039-1367C>T	ENSP00000361971.1:n.1039-1367C>T
ENST00000478995.1:n.229C>T
ENST00000618050.4:c.1557C>T	ENSP00000479125.1:p.His519=
ENST00000621635.4:c.1659C>T	ENSP00000483570.1:p.His553=
NM_000061.2:c.1557C>T , LRG_128t1:c.1557C>T	NP_000052.1:p.His519=
NM_001287344.1:c.1659C>T	NP_001274273.1:p.His553=
NM_001287345.1:c.1039-1367C>T	NP_001274274.1:n.1039-1367C>T
NM_000061.3:c.1557C>T MANE Select	NP_000052.1:p.His519=
NM_001287344.2:c.1659C>T	NP_001274273.1:p.His553=
NM_001287345.2:c.1039-1367C>T	NP_001274274.1:n.1039-1367C>T