Canonical Allele Identifier: CA313526

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63349774A>C , CM000682.2:g.63349774A>C	GRCh38
NC_000020.10:g.61981126A>C , CM000682.1:g.61981126A>C	GRCh37
NC_000020.9:g.61451570A>C	NCBI36
NG_011931.1:g.16570T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.1637T>G MANE Select	ENSP00000359285.4:p.Val546Gly
ENST00000370263.8:c.1637T>G	ENSP00000359285.4:p.Val546Gly
ENST00000463705.5:n.2285T>G
ENST00000467563.3:n.1707T>G
ENST00000498043.6:c.1661T>G
ENST00000615287.4:c.1424T>G	ENSP00000483388.1:p.Val475Gly
ENST00000627000.1:c.*1326T>G	ENSP00000486914.1:n.*1326T>G
ENST00000630240.1:n.1358T>G
NM_000744.6:c.1637T>G	NP_000735.1:p.Val546Gly
NM_001256573.1:c.1109T>G	NP_001243502.1:p.Val370Gly
NR_046317.1:n.1893T>G
XM_011528524.1:c.1424T>G	XP_011526826.1:p.Val475Gly
XM_017027625.2:c.1109T>G	XP_016883114.1:p.Val370Gly
XM_024451822.1:c.1109T>G	XP_024307590.1:p.Val370Gly
NM_001256573.2:c.1109T>G	NP_001243502.1:p.Val370Gly
NR_046317.2:n.1846T>G
NM_000744.7:c.1637T>G MANE Select	NP_000735.1:p.Val546Gly