Canonical Allele Identifier: CA313625

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63346775C>A , CM000682.2:g.63346775C>A	GRCh38
NC_000020.10:g.61978127C>A , CM000682.1:g.61978127C>A	GRCh37
NC_000020.9:g.61448571C>A	NCBI36
NG_011931.1:g.19569G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.1847G>T MANE Select	ENSP00000359285.4:p.Gly616Val
ENST00000370263.8:c.1847G>T	ENSP00000359285.4:p.Gly616Val
ENST00000463705.5:n.2495G>T
ENST00000467563.3:n.1917G>T
ENST00000498043.6:c.1871G>T
ENST00000615287.4:c.1634G>T	ENSP00000483388.1:p.Gly545Val
ENST00000627000.1:c.*1536G>T	ENSP00000486914.1:n.*1536G>T
ENST00000631289.1:n.161G>T
NM_000744.6:c.1847G>T	NP_000735.1:p.Gly616Val
NM_001256573.1:c.1319G>T	NP_001243502.1:p.Gly440Val
NR_046317.1:n.2103G>T
XM_011528524.1:c.1634G>T	XP_011526826.1:p.Gly545Val
XM_017027625.2:c.1319G>T	XP_016883114.1:p.Gly440Val
XM_024451822.1:c.1319G>T	XP_024307590.1:p.Gly440Val
NM_001256573.2:c.1319G>T	NP_001243502.1:p.Gly440Val
NR_046317.2:n.2056G>T
NM_000744.7:c.1847G>T MANE Select	NP_000735.1:p.Gly616Val