Canonical Allele Identifier: CA413925639

Gene: BTK

Linked Data

• MyVariant Identifiers: chrX:g.100611926G>C (hg19) ; chrX:g.101356938G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101356938G>C , CM000685.2:g.101356938G>C	GRCh38
NC_000023.10:g.100611926G>C , CM000685.1:g.100611926G>C	GRCh37
NC_000023.9:g.100498582G>C	NCBI36
NG_009616.1:g.34287C>G , LRG_128:g.34287C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478995.2:n.1355C>G
ENST00000488970.2:n.1353C>G
ENST00000695614.1:c.1195C>G	ENSP00000512053.1:p.Pro399Ala
ENST00000695615.1:c.1195C>G	ENSP00000512054.1:p.Pro399Ala
ENST00000695616.1:c.*1040C>G	ENSP00000512055.1:n.*1040C>G
ENST00000695617.1:c.1192C>G	ENSP00000512056.1:p.Pro398Ala
ENST00000695618.1:c.*944C>G	ENSP00000512058.1:n.*944C>G
ENST00000695619.1:c.*905C>G	ENSP00000512059.1:n.*905C>G
ENST00000695620.1:c.*1040C>G	ENSP00000512060.1:n.*1040C>G
ENST00000695621.1:c.1195C>G	ENSP00000512061.1:p.Pro399Ala
ENST00000695622.1:c.1132C>G	ENSP00000512062.1:p.Pro378Ala
ENST00000695623.1:c.1189C>G	ENSP00000512063.1:p.Pro397Ala
ENST00000695624.1:n.500C>G
ENST00000695625.1:c.1195C>G	ENSP00000512064.1:p.Pro399Ala
ENST00000695626.1:c.191-24C>G	ENSP00000512065.1:n.191-24C>G
ENST00000695627.1:c.208C>G	ENSP00000512066.1:p.Pro70Ala
ENST00000695628.1:c.190+571C>G	ENSP00000512067.1:n.190+571C>G
ENST00000695629.1:c.190+571C>G	ENSP00000512068.1:n.190+571C>G
ENST00000695630.1:c.204C>G
ENST00000695631.1:c.114+1372C>G
ENST00000695632.1:n.212C>G
ENST00000703407.1:c.1038+1436C>G	ENSP00000512057.1:n.1038+1436C>G
ENST00000308731.8:c.1195C>G MANE Select	ENSP00000308176.8:p.Pro399Ala
ENST00000308731.7:c.1195C>G	ENSP00000308176.7:p.Pro399Ala
ENST00000372880.5:c.1038+1436C>G	ENSP00000361971.1:n.1038+1436C>G
ENST00000470329.1:n.145C>G
ENST00000618050.4:c.1195C>G	ENSP00000479125.1:p.Pro399Ala
ENST00000621635.4:c.1297C>G	ENSP00000483570.1:p.Pro433Ala
NM_000061.2:c.1195C>G , LRG_128t1:c.1195C>G	NP_000052.1:p.Pro399Ala
NM_001287344.1:c.1297C>G	NP_001274273.1:p.Pro433Ala
NM_001287345.1:c.1038+1436C>G	NP_001274274.1:n.1038+1436C>G
NM_000061.3:c.1195C>G MANE Select	NP_000052.1:p.Pro399Ala
NM_001287344.2:c.1297C>G	NP_001274273.1:p.Pro433Ala
NM_001287345.2:c.1038+1436C>G	NP_001274274.1:n.1038+1436C>G